Amlodipine and Benazepril Hydrochloride
- Product NDC
- 68071-4524
- 11-digit product format
- 680714524
- Labeler code
- 68071
- Product ID
- 68071-4524_bbb840fe-300b-214d-e053-2995a90a6561
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine and Benazepril Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA202239
- Marketing category
- ANDA
- Marketing start
- 2012-09-05
- Marketing end
- 0000-00-00
- Substance
- AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
- Active strength
- 5 mg/1; mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS],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 |
|---|
| 68071-4524-3 | 68071452403 | 30 CAPSULE in 1 BOTTLE (68071-4524-3) | 30 capsule | 2018-08-13 | 0000-00-00 | No | No | Current |
| 68071-4524-6 | 68071452406 | 60 CAPSULE in 1 BOTTLE (68071-4524-6) | 60 capsule | 2018-08-13 | 0000-00-00 | No | No | Current |
| 68071-4524-9 | 68071452409 | 90 CAPSULE in 1 BOTTLE (68071-4524-9) | 90 capsule | 2018-08-13 | 0000-00-00 | No | No | Current |