Losartan potassium Tablets, 50 mg
- Product NDC
- 42291-423
- 11-digit product format
- 422910423
- Labeler code
- 42291
- Product ID
- 42291-423_d57cc46b-0b90-113d-e053-2995a90a92e4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- losartan potassium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA201170
- Marketing category
- ANDA
- Marketing start
- 2018-10-23
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42291-423-10 | 42291042310 | 1000 TABLET in 1 BOTTLE (42291-423-10) | 1000 tablet | 2018-10-23 | 0000-00-00 | No | No | Current |