Valsartan
- Product NDC
- 70518-1279
- 11-digit product format
- 705181279
- Labeler code
- 70518
- Product ID
- 70518-1279_9129b0a4-b054-022d-e053-2995a90afca7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valsartan
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA202696
- Marketing category
- ANDA
- Marketing start
- 2018-06-29
- Marketing end
- 0000-00-00
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record