Losartan Potassium
- Product NDC
- 50090-5481
- 11-digit product format
- 500905481
- Labeler code
- 50090
- Product ID
- 50090-5481_335a67cc-f563-47e8-861d-c471c3678628
- 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
- 2017-11-01
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5481-0 | 50090548100 | 90 TABLET in 1 BOTTLE (50090-5481-0) | 90 tablet | 2021-03-08 | 0000-00-00 | No | No | Current |