Benazepril Hydrochloride and Hydrochlorothiazide
- Product NDC
- 63629-2680
- 11-digit product format
- 636292680
- Labeler code
- 63629
- Product ID
- 63629-2680_dc00e0fc-3f68-4608-7dc1-2ca800827a6d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benazepril Hydrochloride and Hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076631
- Marketing category
- ANDA
- Marketing start
- 2004-02-11
- 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
- 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 |
|---|
| 63629-2680-1 | 63629268001 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-2680-1) | 2008-09-15 | 0000-00-00 | No | No | Current |
| 63629-2680-2 | 63629268002 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-2680-2) | 2007-12-11 | 0000-00-00 | No | No | Current |
| 63629-2680-3 | 63629268003 | 100 TABLET, FILM COATED in 1 BOTTLE (63629-2680-3) | 2008-11-14 | 0000-00-00 | No | No | Current |
| 63629-2680-4 | 63629268004 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-2680-4) | 2022-04-29 | 0000-00-00 | No | No | Current |