Amlodipine Besylate
- Product NDC
- 63629-8023
- 11-digit product format
- 636298023
- Labeler code
- 63629
- Product ID
- 63629-8023_f389d813-3b78-4d7c-97bf-008913d4abbd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine Besylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA203245
- Marketing category
- ANDA
- Marketing start
- 2014-03-03
- Marketing end
- 0000-00-00
- Substance
- AMLODIPINE BESYLATE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 63629-8023-1 | 63629802301 | 90 TABLET in 1 BOTTLE (63629-8023-1) | 90 tablet | 2019-07-25 | 0000-00-00 | No | No | Current |
| 63629-8023-2 | 63629802302 | 30 TABLET in 1 BOTTLE (63629-8023-2) | 30 tablet | 2019-07-25 | 0000-00-00 | No | No | Current |