Valsartan and Hydrochlorothiazide
- Product NDC
- 68071-4184
- 11-digit product format
- 680714184
- Labeler code
- 68071
- Product ID
- 68071-4184_d5cbb80c-c31e-ac08-e053-2995a90a264d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valsartan and Hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- 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
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 |
|---|
| 68071-4184-3 | 68071418403 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-4184-3) | 2017-12-11 | 0000-00-00 | No | No | Current |
| 68071-4184-6 | 68071418406 | 60 TABLET, FILM COATED in 1 BOTTLE (68071-4184-6) | 2017-12-11 | 0000-00-00 | No | No | Current |