Valsartan and Hydrochlorothiazide
- Product NDC
- 50268-792
- 11-digit product format
- 502680792
- Labeler code
- 50268
- Product ID
- 50268-792_6dd20ee1-7314-a4ba-e053-2991aa0a7a5b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valsartan and Hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- AvPAK
- Application
- ANDA078946
- Marketing category
- ANDA
- Marketing start
- 2016-08-01
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE; VALSARTAN
- Active strength
- 25 mg/1; mg/1
- Pharmacologic classes
- Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record