Benazepril Hydrochloride
- Product NDC
- 68071-5088
- 11-digit product format
- 680715088
- Labeler code
- 68071
- Product ID
- 68071-5088_bbf27a35-62a1-1c29-e053-2a95a90a1f54
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benazepril Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA076820
- Marketing category
- ANDA
- Marketing start
- 2010-02-02
- Marketing end
- 0000-00-00
- Substance
- BENAZEPRIL HYDROCHLORIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-5088-0 | 68071508800 | 100 TABLET in 1 BOTTLE (68071-5088-0) | 100 tablet | 2019-10-18 | 0000-00-00 | No | No | Current |