benazepril hydrochloride and hydrochlorothiazide
- Product NDC
- 60429-405
- 11-digit product format
- 604290405
- Labeler code
- 60429
- Product ID
- 60429-405_b5fbb486-f5cb-3166-e053-2a95a90a70b2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- benazepril hydrochloride and hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA078794
- Marketing category
- ANDA
- Marketing start
- 2014-08-21
- Marketing end
- 0000-00-00
- Substance
- BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
- Active strength
- 20 mg/1; mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE],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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60429-405-01 | 60429040501 | 100 TABLET in 1 BOTTLE (60429-405-01) | 100 tablet | 2015-02-09 | 0000-00-00 | No | No | Current |