Losartan Potassium
- Product NDC
- 68788-7365
- 11-digit product format
- 687887365
- Labeler code
- 68788
- Product ID
- 68788-7365_e8b70250-e397-4e7b-8331-84f603708d10
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA076958
- Marketing category
- ANDA
- Marketing start
- 2011-03-21
- Marketing end
- 0000-00-00
- Substance
- LOSARTAN POTASSIUM
- Active strength
- 50 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