Losartan Potassium
- Product NDC
- 68788-7386
- 11-digit product format
- 687887386
- Labeler code
- 68788
- Product ID
- 68788-7386_ff326dd3-0026-4673-8d32-80a18bc19637
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA091497
- Marketing category
- ANDA
- Marketing start
- 2016-09-08
- 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
- 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 |
|---|
| 68788-7386-1 | 68788738601 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-7386-1) | 2016-09-08 | 0000-00-00 | No | No | Current |
| 68788-7386-3 | 68788738603 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7386-3) | 2016-09-08 | 0000-00-00 | No | No | Current |
| 68788-7386-6 | 68788738606 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-7386-6) | 2016-09-08 | 0000-00-00 | No | No | Current |
| 68788-7386-9 | 68788738609 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7386-9) | 2016-09-08 | 0000-00-00 | No | No | Current |