Valsartan
- Product NDC
- 50090-6347
- 11-digit product format
- 500906347
- Labeler code
- 50090
- Product ID
- 50090-6347_cfddbd29-f63f-476d-a919-4f10dd485a9b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valsartan
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA203311
- Marketing category
- ANDA
- Marketing start
- 2021-06-23
- Substance
- VALSARTAN
- Active strength
- 80 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 |
|---|
| 50090-6347-0 | 50090634700 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-6347-0) | 2023-01-25 | No | No | Historical |
| 50090-6347-1 | 50090634701 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-6347-1) | 2023-01-25 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Valsartan | A-S Medication Solutions | 2023-01-31 | HUMAN PRESCRIPTION DRUG LABEL | 1 |