LOSARTAN POTASSIUM
- Product NDC
- 62980-501
- 11-digit product format
- 629800501
- Labeler code
- 62980
- Product ID
- 62980-501_c86f6112-1ed8-44a7-a240-3b5fed85cc67
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LOSARTAN POTASSIUM
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL; ORAL; ORAL; ORAL; ORAL
- Labeler
- Vivimed Labs Limited
- Application
- ANDA090382
- Marketing category
- ANDA
- Marketing start
- 2014-03-11
- Marketing end
- 0000-00-00
- Substance
- LOSARTAN POTASSIUM
- Active strength
- 25 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record