Valsartan
- Product NDC
- 63629-6922
- 11-digit product format
- 636296922
- Labeler code
- 63629
- Product ID
- 63629-6922_9b59d301-8886-4408-a06a-f1f69289101f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- valsartan
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA021283
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2014-07-07
- Marketing end
- 0000-00-00
- Substance
- VALSARTAN
- Active strength
- 80 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-6922-1 | 63629692201 | 30 TABLET in 1 BOTTLE (63629-6922-1) | 30 tablet | 2016-02-18 | 0000-00-00 | No | No | Current |
| 63629-6922-2 | 63629692202 | 90 TABLET in 1 BOTTLE (63629-6922-2) | 90 tablet | 2016-02-18 | 0000-00-00 | No | No | Current |
| 63629-6922-3 | 63629692203 | 60 TABLET in 1 BOTTLE (63629-6922-3) | 60 tablet | 2016-02-18 | 0000-00-00 | No | No | Current |
| 63629-6922-4 | 63629692204 | 28 TABLET in 1 BOTTLE (63629-6922-4) | 28 tablet | 2016-02-18 | 0000-00-00 | No | No | Current |