Losatan Potassium
- Product NDC
- 70518-0862
- 11-digit product format
- 705180862
- Labeler code
- 70518
- Product ID
- 70518-0862_8eefec5c-f649-054b-e053-2995a90a8dcb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losatan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090428
- Marketing category
- ANDA
- Marketing start
- 2017-11-22
- 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