Losartan Potassium
- Product NDC
- 55700-474
- 11-digit product format
- 557000474
- Labeler code
- 55700
- Product ID
- 55700-474_6ea81244-0cae-44a6-9070-4e037c1a36b0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA091497
- Marketing category
- ANDA
- Marketing start
- 2017-01-13
- Marketing end
- 0000-00-00
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record