Losartan Potassium
- Product NDC
- 50090-3231
- 11-digit product format
- 500903231
- Labeler code
- 50090
- Product ID
- 50090-3231_6c21d15b-bc6a-4b42-aa1c-29bbdc45a376
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078232
- Marketing category
- ANDA
- Marketing start
- 2010-10-06
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record