AMLODIPINE BESYLATE
- Product NDC
- 68788-6935
- 11-digit product format
- 687886935
- Labeler code
- 68788
- Product ID
- 68788-6935_5f652cbc-2a36-4b48-980f-202ee3780a2a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMLODIPINE BESYLATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA077073
- Marketing category
- ANDA
- Marketing start
- 2017-03-28
- Marketing end
- 0000-00-00
- Substance
- AMLODIPINE BESYLATE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 68788-6935-1 | 68788693501 | 100 TABLET in 1 BOTTLE (68788-6935-1) | 100 tablet | 2017-03-28 | 0000-00-00 | No | No | Current |
| 68788-6935-3 | 68788693503 | 30 TABLET in 1 BOTTLE (68788-6935-3) | 30 tablet | 2017-03-28 | 0000-00-00 | No | No | Current |
| 68788-6935-6 | 68788693506 | 60 TABLET in 1 BOTTLE (68788-6935-6) | 60 tablet | 2017-03-28 | 0000-00-00 | No | No | Current |
| 68788-6935-9 | 68788693509 | 90 TABLET in 1 BOTTLE (68788-6935-9) | 90 tablet | 2017-03-28 | 0000-00-00 | No | No | Current |