Valsartan and Hydrochlorothiazide
- Product NDC
- 63629-7443
- 11-digit product format
- 636297443
- Labeler code
- 63629
- Product ID
- 63629-7443_ab6a7815-9ac6-4ca8-b038-9254ea94418b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valsartan and Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA203145
- Marketing category
- ANDA
- Marketing start
- 2013-04-19
- Marketing end
- 0000-00-00
- Substance
- VALSARTAN; HYDROCHLOROTHIAZIDE
- Active strength
- 160 mg/1; mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
- 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 |
|---|
| 63629-7443-1 | 63629744301 | 30 TABLET in 1 BOTTLE (63629-7443-1) | 30 tablet | 2017-02-28 | 0000-00-00 | No | No | Current |
| 63629-7443-2 | 63629744302 | 90 TABLET in 1 BOTTLE (63629-7443-2) | 90 tablet | 2017-02-28 | 0000-00-00 | No | No | Current |