Valsartan
- Product NDC
- 68788-6882
- 11-digit product format
- 687886882
- Labeler code
- 68788
- Product ID
- 68788-6882_fe3a18ca-1f3a-40d2-bc4b-42e78941c14b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valsartan
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA203311
- Marketing category
- ANDA
- Marketing start
- 2017-01-19
- 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
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record