Losartan potassium
- Product NDC
- 70518-1527
- 11-digit product format
- 705181527
- Labeler code
- 70518
- Product ID
- 70518-1527_93fd0308-4de2-2161-e053-2995a90a56f2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- losartan potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077424
- Marketing category
- ANDA
- Marketing start
- 2018-10-15
- 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