Amlodipine besylate
- Product NDC
- 63629-7642
- 11-digit product format
- 636297642
- Labeler code
- 63629
- Product ID
- 63629-7642_fd129a24-ca5b-46ff-a466-211f4b7ab8ef
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 63629-7642-1 | 63629764201 | 30 TABLET in 1 BOTTLE (63629-7642-1) | 30 tablet | 2018-06-01 | 0000-00-00 | No | No | Current |
| 63629-7642-2 | 63629764202 | 60 TABLET in 1 BOTTLE (63629-7642-2) | 60 tablet | 2018-06-01 | 0000-00-00 | No | No | Current |
| 63629-7642-3 | 63629764203 | 90 TABLET in 1 BOTTLE (63629-7642-3) | 90 tablet | 2018-06-01 | 0000-00-00 | No | No | Current |
| 63629-7642-4 | 63629764204 | 300 TABLET in 1 BOTTLE (63629-7642-4) | 300 tablet | 2018-06-01 | 0000-00-00 | No | No | Current |
| 63629-7642-5 | 63629764205 | 500 TABLET in 1 BOTTLE (63629-7642-5) | 500 tablet | 2018-06-01 | 0000-00-00 | No | No | Current |
| 63629-7642-6 | 63629764206 | 800 TABLET in 1 BOTTLE (63629-7642-6) | 800 tablet | 2018-06-01 | 0000-00-00 | No | No | Current |
| 63629-7642-7 | 63629764207 | 1000 TABLET in 1 BOTTLE (63629-7642-7) | 1000 tablet | 2018-06-01 | 0000-00-00 | No | No | Current |