Valsartan
- Product NDC
- 71335-2151
- 11-digit product format
- 713352151
- Labeler code
- 71335
- Product ID
- 71335-2151_c42a9457-c2f1-4b0b-a954-f67f2ccd1032
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valsartan
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA203311
- Marketing category
- ANDA
- Marketing start
- 2021-06-23
- Substance
- VALSARTAN
- Active strength
- 40 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Valsartan
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| VALSARTAN | 40 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 80M03YXJ7I |
| Rxcui | 349483 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-2151-1 | 71335215101 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2151-1) | 2022-08-22 | 0000-00-00 | No | No | Current |
| 71335-2151-2 | 71335215102 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-2151-2) | 2022-08-22 | 0000-00-00 | No | No | Current |