Losartan Potassium
- Product NDC
- 0179-0202
- 11-digit product format
- 001790202
- Labeler code
- 0179
- Product ID
- 0179-0202_7d79cc2f-a2da-61e8-e053-2a91aa0a8f39
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- KAISER FOUNDATION HOSPITALS
- Application
- ANDA076958
- Marketing category
- ANDA
- Marketing start
- 2016-03-16
- Marketing end
- 2019-08-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record