Valsartan
- Product NDC
- 82804-154
- 11-digit product format
- 828040154
- Labeler code
- 82804
- Product ID
- 82804-154_c64664c5-0981-4086-a933-c9c46d34167f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valsartan
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA203311
- Marketing category
- ANDA
- Marketing start
- 2021-06-23
- Substance
- VALSARTAN
- Active strength
- 160 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 80M03YXJ7I | VALSARTAN | 137862-53-4 | VALSARTAN |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 82804-154-30 | 82804015430 | 30 TABLET, FILM COATED in 1 BOTTLE (82804-154-30) | 2025-02-18 | No | No | Historical |
| 82804-154-90 | 82804015490 | 90 TABLET, FILM COATED in 1 BOTTLE (82804-154-90) | 2024-10-03 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Valsartan | Proficient Rx LP | 2025-02-01 | HUMAN PRESCRIPTION DRUG LABEL | 2 |