Valsartan
- Product NDC
- 63629-7432
- 11-digit product format
- 636297432
- Labeler code
- 63629
- Product ID
- 63629-7432_88e299ec-1915-4d86-bf02-499b30ee228c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valsartan
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202696
- Marketing category
- ANDA
- Marketing start
- 2016-09-19
- Marketing end
- 0000-00-00
- Substance
- VALSARTAN
- Active strength
- 40 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7432-1 | 63629743201 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-7432-1) | 2017-11-03 | 0000-00-00 | No | No | Current |