Amlodipine and Benazepril Hydrochloride
- Product NDC
- 71335-0803
- 11-digit product format
- 713350803
- Labeler code
- 71335
- Product ID
- 71335-0803_fa1a937f-51c8-4198-9e84-d0f49fb5d558
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine and Benazepril Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077179
- Marketing category
- ANDA
- Marketing start
- 2007-05-18
- Marketing end
- 0000-00-00
- Substance
- AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
- Active strength
- 10 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
- 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 |
|---|
| 71335-0803-1 | 71335080301 | 30 CAPSULE in 1 BOTTLE (71335-0803-1) | 30 capsule | 2018-05-09 | 0000-00-00 | No | No | Current |
| 71335-0803-2 | 71335080302 | 60 CAPSULE in 1 BOTTLE (71335-0803-2) | 60 capsule | 2018-05-09 | 0000-00-00 | No | No | Current |
| 71335-0803-3 | 71335080303 | 90 CAPSULE in 1 BOTTLE (71335-0803-3) | 90 capsule | 2018-05-09 | 0000-00-00 | No | No | Current |