ELTIBIO 75

Main information

  • Trade name:
  • ELTIBIO 75 30 TAB
  • Pharmaceutical form:
  • TAB
  • Composition:
  • 30
  • Medicine domain:
  • Humans
  • Medicine type:
  • Allopathic drug

Documents

Localization

  • Available in:
  • ELTIBIO 75 30 TAB
    India
  • Language:
  • English

Other information

Status

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

11-1-2018

Clopidogrel Tablets USP, 75 mg by International Laboratories: Recall - Product Mislabeling

Clopidogrel Tablets USP, 75 mg by International Laboratories: Recall - Product Mislabeling

Missed doses of Clopidogrel increases the risk of heart attack and stroke which can be life threatening.

FDA - U.S. Food and Drug Administration

10-1-2018

International Laboratories, LLC Issues Voluntary Nationwide Recall of one (1) Lot of Clopidogrel Tablets USP, 75 mg packaged in bottles of 30 tablets Due to Mislabeling NDC # 54458-888-16; Lot # 117099A

International Laboratories, LLC Issues Voluntary Nationwide Recall of one (1) Lot of Clopidogrel Tablets USP, 75 mg packaged in bottles of 30 tablets Due to Mislabeling NDC # 54458-888-16; Lot # 117099A

International Laboratories, LLC is voluntarily recalling Lot# 117099A of Clopidogrel Tablets, USP 75 mg, packaged in bottles of 30 tablets, to the consumer level due to mislabeling. The product is labeled as Clopidogrel tablets USP 75 mg but may contain Clopidogrel 75mg or Simvastatin Tablets USP 10 mg.

FDA - U.S. Food and Drug Administration

29-5-2017

Lupin Pharmaceuticals Inc. Announces a Nationwide Recall of Mibelas™ 24 Fe (Norethindrone Acetate and EthinylEstradiol 1mg/0.02mg Chewable Tablets and Ferrous Fumarate 75 mg) Tablets Due to Out of Sequence Tablets and Missing Expiry/Lot Information

Lupin Pharmaceuticals Inc. Announces a Nationwide Recall of Mibelas™ 24 Fe (Norethindrone Acetate and EthinylEstradiol 1mg/0.02mg Chewable Tablets and Ferrous Fumarate 75 mg) Tablets Due to Out of Sequence Tablets and Missing Expiry/Lot Information

Baltimore, Maryland, Lupin Pharmaceuticals Inc. announced today that it has voluntarily recalled lot L600518, Exp 05/18 of Mibelas 24 Fe (Norethindrone Acetate and Ethinyl Estradiol 1 mg/0.02 mg chewable and ferrous fumarate 75 mg) Tablets at the consumer level. A confirmed market complaint indicated a packaging error, where the blister was rotated 180 degrees within the wallet, reversing the weekly tablet orientation and making the lot number and expiration date no longer visible. The first four days of...

FDA - U.S. Food and Drug Administration

7-10-2016

Experts for the European Pharmacopoeia's groups of experts and working parties

Experts for the European Pharmacopoeia's groups of experts and working parties

A very large part of the work related to the drafting of new monographs for the European Pharmacopoeia (EDQM) is carried out by external experts in 75 groups of experts and working parties. Experts for the groups are appointed for a period of three years, and the EDQM is now seeking experts for the period from 2017 to 2019.

Danish Medicines Agency

10-4-2018

RoActemra (Roche Registration GmbH)

RoActemra (Roche Registration GmbH)

RoActemra (Active substance: tocilizumab) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)2179 of Tue, 10 Apr 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/955/T/75

Europe -DG Health and Food Safety

19-3-2018

RANITIDINE 75 MG (Ranitidine) Tablet, Film Coated [Vivimed Labs Limited]

RANITIDINE 75 MG (Ranitidine) Tablet, Film Coated [Vivimed Labs Limited]

Updated Date: Mar 19, 2018 EST

US - DailyMed

28-12-2017

ZANTAC 75 (Ranitidine) Tablet, Coated [Carilion Materials Management]

ZANTAC 75 (Ranitidine) Tablet, Coated [Carilion Materials Management]

Updated Date: Dec 28, 2017 EST

US - DailyMed

8-12-2017

RANITIDINE 75 (Ranitidine Tablets) Tablet [Meijer Distribution Inc]

RANITIDINE 75 (Ranitidine Tablets) Tablet [Meijer Distribution Inc]

Updated Date: Dec 8, 2017 EST

US - DailyMed

8-12-2017

RANITIDINE 75 (Ranitidine Tablets Usp, 75mg) Tablet [The Kroger Co.]

RANITIDINE 75 (Ranitidine Tablets Usp, 75mg) Tablet [The Kroger Co.]

Updated Date: Dec 8, 2017 EST

US - DailyMed

28-11-2017

ACID REDUCER 75 (Ranitidine 75mg) Tablet, Coated [Allegiant Health]

ACID REDUCER 75 (Ranitidine 75mg) Tablet, Coated [Allegiant Health]

Updated Date: Nov 28, 2017 EST

US - DailyMed

26-10-2017

Ingelvac CircoFLEX (Boehringer Ingelheim Vetmedica GmbH)

Ingelvac CircoFLEX (Boehringer Ingelheim Vetmedica GmbH)

Ingelvac CircoFLEX (Active substance: Porcine circovirus type 2 ORF2 protein minimum RP1.0 Maximum RP 3.75) - Centralised - Yearly update - Commission Decision (2017)7264 of Thu, 26 Oct 2017

Europe -DG Health and Food Safety

2-10-2017

Current standards applicable to TGA-licensed HPC manufacturers

Current standards applicable to TGA-licensed HPC manufacturers

TGO 94 Standard for HPCs derived from Cord Blood has replaced TGO 75

Therapeutic Goods Administration - Australia

25-9-2017

ZANTAC 75 (Ranitidine) Tablet [JC World Bell Wholesale Co., Inc.]

ZANTAC 75 (Ranitidine) Tablet [JC World Bell Wholesale Co., Inc.]

Updated Date: Sep 25, 2017 EST

US - DailyMed