Valsartan and Hydrochlorothiazide
- Product NDC
- 71335-0227
- 11-digit product format
- 713350227
- Labeler code
- 71335
- Product ID
- 71335-0227_75fd9a19-d955-4f23-9c8a-6e14327ee311
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valsartan and Hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA203145
- Marketing category
- ANDA
- Marketing start
- 2013-04-19
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE; VALSARTAN
- Active strength
- 13 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0227-1 | 71335022701 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0227-1) | 2018-07-12 | 0000-00-00 | No | No | Current |
| 71335-0227-2 | 71335022702 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0227-2) | 2018-07-25 | 0000-00-00 | No | No | Current |