Amlodipine besylate
- Product NDC
- 63629-1025
- 11-digit product format
- 636291025
- Labeler code
- 63629
- Product ID
- 63629-1025_349a4a00-1e17-4b6a-bb8e-ea2140d979e3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine besylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077955
- Marketing category
- ANDA
- Marketing start
- 2007-11-02
- 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
- 2020-12-31
- 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 |
|---|
| 63629-1025-2 | 63629102502 | 30 TABLET in 1 BOTTLE (63629-1025-2) | 30 tablet | 2007-11-02 | 0000-00-00 | No | No | Current |
| 63629-1025-3 | 63629102503 | 300 TABLET in 1 BOTTLE (63629-1025-3) | 300 tablet | 2007-11-02 | 0000-00-00 | No | No | Current |
| 63629-1025-5 | 63629102505 | 500 TABLET in 1 BOTTLE (63629-1025-5) | 500 tablet | 2007-11-02 | 0000-00-00 | No | No | Current |
| 63629-1025-6 | 63629102506 | 60 TABLET in 1 BOTTLE (63629-1025-6) | 60 tablet | 2007-11-02 | 0000-00-00 | No | No | Current |
| 63629-1025-8 | 63629102508 | 800 TABLET in 1 BOTTLE (63629-1025-8) | 800 tablet | 2007-11-02 | 0000-00-00 | No | No | Current |
| 63629-1025-9 | 63629102509 | 90 TABLET in 1 BOTTLE (63629-1025-9) | 90 tablet | 2018-06-01 | 0000-00-00 | No | No | Current |