Valsartan and Hydrochlorothiazide
- Product NDC
- 50090-4839
- 11-digit product format
- 500904839
- Labeler code
- 50090
- Product ID
- 50090-4839_fe4f19ce-4447-422e-9bfc-f71da077aed4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valsartan and Hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA201662
- Marketing category
- ANDA
- Marketing start
- 2016-05-20
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-4839 | VALSARTAN AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 5 | Legacy NDC | 20230208_f2f5e63e-0340-499b-bade-6a89d596ba90.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4839-0 | 50090483900 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-4839-0) | 2020-01-20 | 0000-00-00 | No | No | Current |
| 50090-4839-1 | 50090483901 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-4839-1) | 2020-01-20 | 0000-00-00 | No | No | Current |