Amlodipine Besylate and Benazepril Hydrochloride
- Product NDC
- 63629-7643
- 11-digit product format
- 636297643
- Labeler code
- 63629
- Product ID
- 63629-7643_aab4b82c-24bd-484a-8f4d-0e190f2a0a9d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine Besylate and Benazepril Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077183
- Marketing category
- ANDA
- Marketing start
- 2010-04-19
- Marketing end
- 0000-00-00
- Substance
- AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
- Active strength
- 3 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 63629-7643-1 | 63629764301 | 30 CAPSULE in 1 BOTTLE (63629-7643-1) | 30 capsule | 2018-06-08 | 0000-00-00 | No | No | Current |
| 63629-7643-2 | 63629764302 | 90 CAPSULE in 1 BOTTLE (63629-7643-2) | 90 capsule | 2018-06-08 | 0000-00-00 | No | No | Current |