Amlodipine Besylate and Benazepril Hydrochloride
- Product NDC
- 50090-1463
- 11-digit product format
- 500901463
- Labeler code
- 50090
- Product ID
- 50090-1463_2d73d3ea-82e4-4f17-bc0f-9102cec17877
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine Besylate and Benazepril Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090149
- Marketing category
- ANDA
- Marketing start
- 2011-07-05
- 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
- 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 |
|---|
| 50090-1463-0 | 50090146300 | 90 CAPSULE in 1 BOTTLE (50090-1463-0) | 90 capsule | 2014-11-28 | 0000-00-00 | No | No | Current |