Losartan Potassium
- Product NDC
- 68645-411
- 11-digit product format
- 686450411
- Labeler code
- 68645
- Product ID
- 68645-411_158d10b1-a1f5-4725-bb56-9e6dadaae1dd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Legacy Pharmaceutical Packaging, LLC
- Application
- ANDA076958
- Marketing category
- ANDA
- Marketing start
- 2010-04-06
- Marketing end
- 2019-09-30
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record