Valsartan
- Product NDC
- 0591-2169
- 11-digit product format
- 005912169
- Labeler code
- 0591
- Product ID
- 0591-2169_70122f99-a4e4-4c32-8c5c-d843df4a974e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- valsartan
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Actavis Pharma, Inc.
- Application
- ANDA090642
- Marketing category
- ANDA
- Marketing start
- 2015-01-05
- Marketing end
- 2019-08-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record