VALSARTAN
- Product NDC
- 43353-203
- 11-digit product format
- 433530203
- Labeler code
- 43353
- Product ID
- 43353-203_5d9f8837-554b-4b8e-ada3-7e705d4806d0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- VALSARTAN
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA077492
- Marketing category
- ANDA
- Marketing start
- 2014-07-07
- Marketing end
- 0000-00-00
- Substance
- VALSARTAN
- Active strength
- 320 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 80M03YXJ7I | VALSARTAN | 137862-53-4 | VALSARTAN |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| VALSARTAN | Aphena Pharma Solutions - Tennessee, LLC | 2016-07-13 | HUMAN PRESCRIPTION DRUG LABEL | 1 |