Losartan Potassium
- Product NDC
- 68788-6333
- 11-digit product format
- 687886333
- Labeler code
- 68788
- Product ID
- 68788-6333_a748835f-589e-4a9b-a074-73f69996b80c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- losartan potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA091497
- Marketing category
- ANDA
- Marketing start
- 2016-10-17
- Marketing end
- 0000-00-00
- Substance
- LOSARTAN POTASSIUM
- Active strength
- 100 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record