Losartan Potassium
- Product NDC
- 55700-769
- 11-digit product format
- 557000769
- Labeler code
- 55700
- Product ID
- 55700-769_697e1aa0-b1d7-4983-8078-13f012fbbd82
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA090083
- Marketing category
- ANDA
- Marketing start
- 2019-06-28
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-769-90 | 55700076990 | 90 TABLET, FILM COATED in 1 BOTTLE (55700-769-90) | 2019-06-28 | 0000-00-00 | No | No | Current |