Losartan Potassium
- Product NDC
- 71335-0884
- 11-digit product format
- 713350884
- Labeler code
- 71335
- Product ID
- 71335-0884_ec4087c8-8ad7-4bfb-afa4-b300341e67c7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA091497
- Marketing category
- ANDA
- Marketing start
- 2011-06-01
- Marketing end
- 0000-00-00
- Substance
- LOSARTAN POTASSIUM
- Active strength
- 25 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 71335-0884-1 | 71335088401 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0884-1) | 2016-12-22 | 0000-00-00 | No | No | Current |
| 71335-0884-2 | 71335088402 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0884-2) | 2016-12-22 | 0000-00-00 | No | No | Current |
| 71335-0884-3 | 71335088403 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0884-3) | 2016-12-22 | 0000-00-00 | No | No | Current |
| 71335-0884-4 | 71335088404 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-0884-4) | 2016-12-22 | 0000-00-00 | No | No | Current |