Amlodipine Besylate
- Product NDC
- 63629-7640
- 11-digit product format
- 636297640
- Labeler code
- 63629
- Product ID
- 63629-7640_716bd50c-fd0f-4022-b049-0d194f3dddb7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine besylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078925
- Marketing category
- ANDA
- Marketing start
- 2010-10-20
- Marketing end
- 0000-00-00
- Substance
- AMLODIPINE BESYLATE
- Active strength
- 3 mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 63629-7640-1 | 63629764001 | 30 TABLET in 1 BOTTLE (63629-7640-1) | 30 tablet | 2014-04-17 | 0000-00-00 | No | No | Current |
| 63629-7640-2 | 63629764002 | 60 TABLET in 1 BOTTLE (63629-7640-2) | 60 tablet | 2014-04-17 | 0000-00-00 | No | No | Current |
| 63629-7640-3 | 63629764003 | 90 TABLET in 1 BOTTLE (63629-7640-3) | 90 tablet | 2014-04-17 | 0000-00-00 | No | No | Current |
| 63629-7640-4 | 63629764004 | 300 TABLET in 1 BOTTLE (63629-7640-4) | 300 tablet | 2014-04-17 | 0000-00-00 | No | No | Current |
| 63629-7640-5 | 63629764005 | 500 TABLET in 1 BOTTLE (63629-7640-5) | 500 tablet | 2014-04-17 | 0000-00-00 | No | No | Current |
| 63629-7640-6 | 63629764006 | 800 TABLET in 1 BOTTLE (63629-7640-6) | 800 tablet | 2014-04-17 | 0000-00-00 | No | No | Current |
| 63629-7640-7 | 63629764007 | 1000 TABLET in 1 BOTTLE (63629-7640-7) | 1000 tablet | 2014-04-17 | 0000-00-00 | No | No | Current |