LOSARTAN POTASSIUM
- Product NDC
- 71335-1082
- 11-digit product format
- 713351082
- Labeler code
- 71335
- Product ID
- 71335-1082_05b4b16f-e350-48ab-95e8-5702841a5c2f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LOSARTAN POTASSIUM
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090382
- Marketing category
- ANDA
- Marketing start
- 2018-01-04
- Marketing end
- 0000-00-00
- Substance
- LOSARTAN POTASSIUM
- Active strength
- 100 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 |
|---|
| 71335-1082-1 | 71335108201 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1082-1) | 2019-02-07 | 0000-00-00 | No | No | Current |
| 71335-1082-2 | 71335108202 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1082-2) | 2019-02-07 | 0000-00-00 | No | No | Current |
| 71335-1082-3 | 71335108203 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1082-3) | 2019-02-07 | 0000-00-00 | No | No | Current |
| 71335-1082-4 | 71335108204 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-1082-4) | 2019-02-07 | 0000-00-00 | No | No | Current |
| 71335-1082-5 | 71335108205 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-1082-5) | 2019-02-07 | 0000-00-00 | No | No | Current |
| 71335-1082-6 | 71335108206 | 28 TABLET, FILM COATED in 1 BOTTLE (71335-1082-6) | 2019-02-07 | 0000-00-00 | No | No | Current |
| 71335-1082-7 | 71335108207 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-1082-7) | 2019-02-07 | 0000-00-00 | No | No | Current |