ESLOVA
Main information
- Trade name:
- ESLOVA 10 TAB
- Active ingredient:
- S-Amlodipine,ATORVASTATIN
- Available from:
- Zuventus
- Dosage:
- 5,10;MG
- Pharmaceutical form:
- TAB
- Composition:
- 10
- Medicine domain:
- Humans
- Medicine type:
- Allopathic drug
Documents
- for the general public:
- The information leaflet for this product is not currently available, you can send a request to our customer service and we will notify you as soon as we are able to obtain it.
Request the information leaflet for the general public.
- for healthcare professionals:
- The information leaflet for this product is not currently available, you can send a request to our customer service and we will notify you as soon as we are able to obtain it.
Request the information leaflet for healthcare professionals.
Localization
- Available in:
-
India
- Language:
- English
Other information
Status
- Source:
- Central Drugs Standard Control Organization
- Last update:
- 09-08-2016
- The information leaflet for this product is not currently available, you can send a request to our customer service and we will notify you as soon as we are able to obtain it.
Request the information leaflet for the general public.
- Access to this document is only available to registered users.
Register now for full access
22-8-2018
UPDATED: Torrent Pharmaceuticals Limited Issues Voluntary Nationwide Recall of Valsartan/Amlodipine/HCTZ, Valsartan/Amlodipine and Valsartan Tablets
Torrent Pharmaceuticals Limited is voluntarily recalling ALL LOTS within expiry of Valsartan/Amlodipine/HCTZ, Valsartan/Amlodipine and Valsartan tablets to the consumer level due to the detection of trace amounts of an unexpected impurity found in an active pharmaceutical ingredient (API) manufactured by Zhejiang Huahai Pharmaceuticals. The impurity detected in the API is N-nitrosodimethylamine (NDMA), which is a substance that occurs naturally in certain foods, drinking water, air pollution, and industr...
FDA - U.S. Food and Drug Administration
18-8-2018
Torrent Pharmaceuticals Limited Issues Voluntary Nationwide Recall of Valsartan / Amlodipine / HCTZ Tablets
Torrent Pharmaceuticals Limited is voluntarily recalling 14 lots of Valsartan/Amlodipine/HCTZ tablets to the consumer level due to the detection of trace amounts of an unexpected impurity found in an active pharmaceutical ingredient (API) manufactured by Zhejiang Huahai Pharmaceuticals. The impurity detected in the API is N-nitrosodimethylamine (NDMA), which is a substance that occurs naturally in certain foods, drinking water, air pollution, and industrial processes, and has been classified as a probabl...
FDA - U.S. Food and Drug Administration
10-8-2018
Human medicines European public assessment report (EPAR): Exforge HCT, amlodipine besylate / valsartan / hydrochlorothiazide, Revision: 13, Authorised
Europe - EMA - European Medicines Agency
5-7-2018
Human medicines European public assessment report (EPAR): Exforge, amlodipine / valsartan, Revision: 21, Authorised
Europe - EMA - European Medicines Agency
4-7-2018
Human medicines European public assessment report (EPAR): Dafiro HCT, amlodipine besylate / valsartan / hydrochlorothiazide, Revision: 13, Authorised
Europe - EMA - European Medicines Agency
19-6-2018
Opinion/decision on a Paediatric investigation plan (PIP): -, Candesartan (cilexetil) / amlodipine (besylate), Therapeutic area: Cardiovascular diseases
Europe - EFSA - European Food Safety Authority EFSA Journal
13-6-2018
Human medicines European public assessment report (EPAR): Copalia HCT, amlodipine / valsartan / hydrochlorothiazide, Revision: 11, Authorised
Europe - EMA - European Medicines Agency
13-6-2018
Human medicines European public assessment report (EPAR): Twynsta, telmisartan / amlodipine, Revision: 9, Authorised
Europe - EMA - European Medicines Agency
12-6-2018
Human medicines European public assessment report (EPAR): Dafiro, amlodipine / valsartan, Revision: 23, Authorised
Europe - EMA - European Medicines Agency
12-6-2018
Human medicines European public assessment report (EPAR): Copalia, amlodipine / valsartan, Revision: 21, Authorised
Europe - EMA - European Medicines Agency
28-5-2018
Human medicines European public assessment report (EPAR): Exforge HCT, amlodipine besylate / valsartan / hydrochlorothiazide, Revision: 12, Authorised
Europe - EMA - European Medicines Agency
14-5-2018
Human medicines European public assessment report (EPAR): Dafiro HCT, amlodipine besylate / valsartan / hydrochlorothiazide, Revision: 12, Authorised
Europe - EMA - European Medicines Agency
14-5-2018
Human medicines European public assessment report (EPAR): Dafiro, amlodipine / valsartan, Revision: 22, Authorised
Europe - EMA - European Medicines Agency
7-5-2018
Human medicines European public assessment report (EPAR): Exforge, amlodipine / valsartan, Revision: 20, Authorised
Europe - EMA - European Medicines Agency
27-6-2018
Copalia HCT (Novartis Europharm Limited)
Copalia HCT (Active substance: amlodipine besylate / valsartan / hydrochlorothiazide) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)4082 of Wed, 27 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/1159/T/67
Europe -DG Health and Food Safety
27-6-2018
Exforge (Novartis Europharm Limited)
Exforge (Active substance: amlodipine / valsartan) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)4085 of Wed, 27 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/716/T/96
Europe -DG Health and Food Safety
27-6-2018
Dafiro HCT (Novartis Europharm Limited)
Dafiro HCT (Active substance: amlodipine besylate / valsartan / hydrochlorothiazide) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)4084 of Wed, 27 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/1160/T/68
Europe -DG Health and Food Safety
11-6-2018
Exforge HCT (Novartis Europharm Limited)
Exforge HCT (Active substance: amlodipine besylate / valsartan / hydrochlorothiazide) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)3752 of Mon, 11 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/1068/T/66
Europe -DG Health and Food Safety
11-6-2018
Dafiro (Novartis Europharm Limited)
Dafiro (Active substance: amlodipine / valsartan) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)3753 of Mon, 11 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/776/T/99
Europe -DG Health and Food Safety
6-6-2018
Copalia (Novartis Europharm Limited)
Copalia (Active substance: amlodipine / valsartan) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)3695 of Wed, 06 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/774/T/97
Europe -DG Health and Food Safety
4-6-2018
Twynsta (Boehringer Ingelheim International GmbH)
Twynsta (Active substance: telmisartan / amlodipine) - Centralised - Yearly update - Commission Decision (2018)3625 of Mon, 04 Jun 2018
Europe -DG Health and Food Safety