Losartan Potassium
- Product NDC
- 68071-3216
- 11-digit product format
- 680713216
- Labeler code
- 68071
- Product ID
- 68071-3216_e4cddf04-1226-42e1-e053-2a95a90afff4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA091497
- Marketing category
- ANDA
- Marketing start
- 2014-07-30
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-3216-1 | 68071321601 | 120 TABLET, FILM COATED in 1 BOTTLE (68071-3216-1) | 2017-05-09 | 0000-00-00 | No | No | Current |
| 68071-3216-6 | 68071321606 | 60 TABLET, FILM COATED in 1 BOTTLE (68071-3216-6) | 2017-05-09 | 0000-00-00 | No | No | Current |
| 68071-3216-9 | 68071321609 | 90 TABLET, FILM COATED in 1 BOTTLE (68071-3216-9) | 2017-05-09 | 0000-00-00 | No | No | Current |