Losartan Potassium
- Product NDC
- 61919-864
- 11-digit product format
- 619190864
- Labeler code
- 61919
- Product ID
- 61919-864_88cb6899-b309-1e93-e053-2995a90a73b0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Direct Rx
- Application
- ANDA090083
- Marketing category
- ANDA
- Marketing start
- 2019-05-13
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-864-90 | 61919086490 | 90 TABLET, FILM COATED in 1 BOTTLE (61919-864-90) | 2019-05-13 | 0000-00-00 | No | No | Current |