ESTUCHOL 150

Main information

  • Trade name:
  • ESTUCHOL 150 10×10
  • Composition:
  • 10×10
  • Medicine domain:
  • Humans
  • Medicine type:
  • Allopathic drug

Documents

Localization

  • Available in:
  • ESTUCHOL 150 10×10
    India
  • Language:
  • English

Other information

Status

  • Source:
  • Central Drugs Standard Control Organization
  • Last update:
  • 09-08-2016

9-4-2018

Club 13 Recalls Kratom Maeng Da Red Powder and Capsules Because of Possible Health Risk

Club 13 Recalls Kratom Maeng Da Red Powder and Capsules Because of Possible Health Risk

Club 13 of St. Augustine, FL is recalling 15-gram, 30-gram, 90-gram, 150-gram, and 454-gram pouches, and all bulk orders of "Maeng Da Red" kratom powder; and 5-count, 25-count, 50-count, 100-count, 120-count capsule, and all bulk capsule orders of “Maeng Da Red” kratom bottles; and 5-count, 20-count, 25-count, 40-count, 50-count capsule “Maeng Da Red XS” kratom bottles because they have the potential to be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections i...

FDA - U.S. Food and Drug Administration

17-1-2018

Baxter Expands Voluntary Nationwide Recall to Include Second Lot of Nexterone Injection Due to Presence of Particulate Matter

Baxter Expands Voluntary Nationwide Recall to Include Second Lot of Nexterone Injection Due to Presence of Particulate Matter

Following the issuance of a voluntary recall dated November 10, 2017 of one lot of NEXTERONE (amiodarone HCl) 150 mg/100 mL Premixed Injection, Baxter International Inc. announced today it is expanding the recall to include a second lot (NC109123) of NEXTERONE due to the potential presence of particulate matter.

FDA - U.S. Food and Drug Administration

30-11-2017

Nutra Labs Inc. Issues Voluntary Nationwide Recall of Dietary Supplements Bull and Chao Jimengnan Tablets Due to Undeclared Active Pharmaceutical Ingredients

Nutra Labs Inc. Issues Voluntary Nationwide Recall of Dietary Supplements Bull and Chao Jimengnan Tablets Due to Undeclared Active Pharmaceutical Ingredients

Nutra Labs Inc. is voluntarily recalling lots sold by their firm of the male enhancement supplements Bull 1800 mg Capsules with the production date of 05/08/2016, and Chao Jimengnan 150 mg Tablets with Lot # 20151018 to the consumer level. FDA analysis found the products to be tainted with sildenafil, 0.026mg/capsule for Bull, and 70.46mg/tablet for Chao Jimengnan respectively. Sildenafil is the active pharmaceutical ingredient in an FDA approved product used for erectile dysfunction, making Bull capsule...

FDA - U.S. Food and Drug Administration

15-11-2017

Nexterone (amiodarone HCl) 150 mg/100 mL Premixed Injection: Recall - Presence Of Particulate Matter

Nexterone (amiodarone HCl) 150 mg/100 mL Premixed Injection: Recall - Presence Of Particulate Matter

Intravenous administration of a solution containing sterile particulate matter may lead to adverse health consequences.

FDA - U.S. Food and Drug Administration

15-11-2017

Baxter Issues A Voluntary Nationwide Recall For One Lot of Nexterone Injection Due To Presence Of Particulate Matter

Baxter Issues A Voluntary Nationwide Recall For One Lot of Nexterone Injection Due To Presence Of Particulate Matter

Baxter International Inc. announced today it is voluntarily recalling one lot of NEXTERONE (amiodarone HCl) 150 mg/100 mL Premixed Injection – distributed between 6/23/2017 and 10/2/2017 in the United States to wholesalers/distributors and healthcare facilities – due to the potential presence of particulate matter. The particulate matter may have entered the solution during the manufacturing process.

FDA - U.S. Food and Drug Administration

1-8-2017

Withdrawal of one more batch of counterfeit packs of the schizophrenia medicine Xeplion 150 mg

Withdrawal of one more batch of counterfeit packs of the schizophrenia medicine Xeplion 150 mg

German and Danish parallel importers and the Danish Medicines Agency are now withdrawing the fourth batch of Xeplion 150 mg from wholesale distributors, hospitals and pharmacies, because the batch contains counterfeit packs.

Danish Medicines Agency

1-8-2017

 Withdrawal of one more batch of counterfeit packs of the schizophrenia medicine Xeplion 150 mg

Withdrawal of one more batch of counterfeit packs of the schizophrenia medicine Xeplion 150 mg

German and Danish parallel importers and the Danish Medicines Agency are now withdrawing the fourth batch of Xeplion 150 mg from wholesale distributors, hospitals and pharmacies, because the batch contains counterfeit packs. The German authorities have informed the Danish Medicines Agency that a German parallel importer has found counterfeit packs in one more batch of Xeplion 150 mg. This batch has also been sold in Denmark and will be withdrawn from the market. We have now withdrawn a total of four ba...

Danish Medicines Agency

27-7-2017

Counterfeit packs of the schizophrenia medicine Xeplion 150 mg

Counterfeit packs of the schizophrenia medicine Xeplion 150 mg

One German and several Danish parallel importers and the Danish Medicines Agency have withdrawn several batches of Xeplion 150 mg from wholesale distributors, hospitals and pharmacies, because the batches contained counterfeit packs.

Danish Medicines Agency

25-7-2017

 Counterfeit packs of the schizophrenia medicine Xeplion 150 mg

Counterfeit packs of the schizophrenia medicine Xeplion 150 mg

Danish parallel importers and the Danish Medicines Agency have withdrawn a batch of Xeplion 150 mg from hospital pharmacies and 26 private pharmacies due to suspicion of falsification. On the basis of the available data, the Danish Medicines Agency assesses that the patient risk is low. Xeplion 150 mg is a medicine for injection used for the treatment of schizophrenia in adults. The medicinal product is available in hospitals or dispensed on prescription at a pharmacy, and usually the patient is inject...

Danish Medicines Agency

23-6-2017

 Substantial progress in cooperation with CFDA only six weeks after state visit

Substantial progress in cooperation with CFDA only six weeks after state visit

Chinese and Danish organisers of the seminar on the licensing of medicines, Beijing June 2017. During the official state visit at the beginning of May, the Chinese and Danish Ministers for Health and Food signed a Memorandum of Understanding about the establishment of the China-Denmark Food and Drug Regulatory Cooperation Centre. Only six weeks after the state visit, the China Food and Drug Administration (CFDA) and the Danish Medicines Agency held a successful seminar on 20 and 21 June in Beijing on t...

Danish Medicines Agency

6-4-2017

More batches of EpiPen® are withdrawn

More batches of EpiPen® are withdrawn

MEDA has decided to withdraw four more batches of EpiPen®. The withdrawal concerns two batches of EpiPen® 300 micrograms/dose and two batches of EpiPen® Jr 150 micrograms/dose. The latter is used for acute hypersensitivity reactions in children. The reason for the withdrawal is that there is a risk that the auto-injector does not work.

Danish Medicines Agency

4-4-2018

ACID REDUCER 150 (Ranitidine) Tablet, Film Coated [HyVee Inc]

ACID REDUCER 150 (Ranitidine) Tablet, Film Coated [HyVee Inc]

Updated Date: Apr 4, 2018 EST

US - DailyMed

3-4-2018

ZANTAC 150 MAXIMUM STRENGTH (Ranitidine Hydrochloride) Tablet [Chattem, Inc.]

ZANTAC 150 MAXIMUM STRENGTH (Ranitidine Hydrochloride) Tablet [Chattem, Inc.]

Updated Date: Apr 3, 2018 EST

US - DailyMed

21-3-2018

EU/3/16/1763 (Quintiles Ireland Limited)

EU/3/16/1763 (Quintiles Ireland Limited)

EU/3/16/1763 (Active substance: Tadekinig alfa) - Transfer of orphan designation - Commission Decision (2018)1825 of Wed, 21 Mar 2018 European Medicines Agency (EMA) procedure number: EMA/OD/150/16/T/01

Europe -DG Health and Food Safety

19-3-2018

RANITIDINE 150 MG (Ranitidine) Tablet, Film Coated [Vivimed Labs Limited]

RANITIDINE 150 MG (Ranitidine) Tablet, Film Coated [Vivimed Labs Limited]

Updated Date: Mar 19, 2018 EST

US - DailyMed

14-3-2018

VITAMIN B COMPLEX 150 (Vitamin B Complex) Injection [Butler Animal Health Supply LLC]

VITAMIN B COMPLEX 150 (Vitamin B Complex) Injection [Butler Animal Health Supply LLC]

Updated Date: Mar 14, 2018 EST

US - DailyMed

2-3-2018

UP AND UP RANITIDINE 150 (Ranitidine) Tablet, Film Coated [Target Corporation]

UP AND UP RANITIDINE 150 (Ranitidine) Tablet, Film Coated [Target Corporation]

Updated Date: Mar 2, 2018 EST

US - DailyMed

26-2-2018

EU/3/18/1976 (UniversitAtsmedizin der Johannes Gutenberg-UniversitAt Mainz)

EU/3/18/1976 (UniversitAtsmedizin der Johannes Gutenberg-UniversitAt Mainz)

EU/3/18/1976 (Active substance: Allogeneic CD4+ and CD25+ T lymphocytes ex vivo incubated with GP120) - Orphan designation - Commission Decision (2018)1243 of Mon, 26 Feb 2018 European Medicines Agency (EMA) procedure number: EMA/OD/150/17

Europe -DG Health and Food Safety

14-2-2018

BOVA PRO 150 ARCTIC GUARD (Iodine) Solution [AgroChem Inc.]

BOVA PRO 150 ARCTIC GUARD (Iodine) Solution [AgroChem Inc.]

Updated Date: Feb 14, 2018 EST

US - DailyMed

31-1-2018

Scientific guideline:  Draft vismodegib hard capsule 150 mg product-specific bioequivalence guidance, draft: consultation open

Scientific guideline: Draft vismodegib hard capsule 150 mg product-specific bioequivalence guidance, draft: consultation open

Vismodegib hard capsule 150 mg product-specific bioequivalence guidance

Europe - EMA - European Medicines Agency

15-12-2017

ZANTAC 150 ACID REDUCER (Ranitidine) Tablet [Lil' Drug Store Products, Inc]

ZANTAC 150 ACID REDUCER (Ranitidine) Tablet [Lil' Drug Store Products, Inc]

Updated Date: Dec 15, 2017 EST

US - DailyMed

11-12-2017

ACID REDUCER 150 (Ranitidine Hydrochloride Tablets 150mg) Tablet, Coated [Safeway Inc]

ACID REDUCER 150 (Ranitidine Hydrochloride Tablets 150mg) Tablet, Coated [Safeway Inc]

Updated Date: Dec 11, 2017 EST

US - DailyMed

16-11-2017

RANITIDINE 150 (Ranitidine Hcl Tablets 150mg) Tablet, Coated [Allegiant Health]

RANITIDINE 150 (Ranitidine Hcl Tablets 150mg) Tablet, Coated [Allegiant Health]

Updated Date: Nov 16, 2017 EST

US - DailyMed

15-11-2017

RANITIDINE 150 (Ranitidine Hcl Tablets 150mg) Tablet, Coated [Marc Glassman, Inc.]

RANITIDINE 150 (Ranitidine Hcl Tablets 150mg) Tablet, Coated [Marc Glassman, Inc.]

Updated Date: Nov 15, 2017 EST

US - DailyMed

8-11-2017

WAL-ZAN (Ranitidine Hydrochloride Tablets 150mg) Tablet, Coated [Walgreens Company]

WAL-ZAN (Ranitidine Hydrochloride Tablets 150mg) Tablet, Coated [Walgreens Company]

Updated Date: Nov 8, 2017 EST

US - DailyMed

18-10-2017

HARRIS TEETER ACID REDUCER 150 (Ranitidine) Tablet, Film Coated [Harris Teeter, LLC]

HARRIS TEETER ACID REDUCER 150 (Ranitidine) Tablet, Film Coated [Harris Teeter, LLC]

Updated Date: Oct 18, 2017 EST

US - DailyMed

25-9-2017

ZANTAC 150 (Ranitidine) Tablet [JC World Bell Wholesale Co., Inc.]

ZANTAC 150 (Ranitidine) Tablet [JC World Bell Wholesale Co., Inc.]

Updated Date: Sep 25, 2017 EST

US - DailyMed

31-8-2017

BASIC CARE ACID REDUCER 150 (Ranitidine) Tablet, Film Coated [L. Perrigo Company]

BASIC CARE ACID REDUCER 150 (Ranitidine) Tablet, Film Coated [L. Perrigo Company]

Updated Date: Aug 31, 2017 EST

US - DailyMed

17-8-2017

CLEAR SALVE 150 (Salicylic Acid) Salve [Ceela Naturals]

CLEAR SALVE 150 (Salicylic Acid) Salve [Ceela Naturals]

Updated Date: Aug 17, 2017 EST

US - DailyMed

8-8-2017

Paracetamol / ibuprofen 500 mg / 150 mg Film-coated tablets (Paracomb)

Paracetamol / ibuprofen 500 mg / 150 mg Film-coated tablets (Paracomb)

Paracetamol / ibuprofen 500 mg / 150 mg Film-coated tablets (Paracomb) (Active substance: paracetamol / ibuprofen) - Community Referrals - Art 29 - Commission Decision (2017) 5646 of Tue, 08 Aug 2017 European Medicines Agency (EMA) procedure number: EMEA/H/A-29(4)/1447

Europe -DG Health and Food Safety

25-4-2017

150-Year-Old Drug May Shorten 'Off' Time for Parkinson's Patients

150-Year-Old Drug May Shorten 'Off' Time for Parkinson's Patients

Title: 150-Year-Old Drug May Shorten 'Off' Time for Parkinson's PatientsCategory: Health NewsCreated: 4/21/2017 12:00:00 AMLast Editorial Review: 4/24/2017 12:00:00 AM

US - MedicineNet