AMLODIPINE BESYLATE
- Product NDC
- 68071-3188
- 11-digit product format
- 680713188
- Labeler code
- 68071
- Product ID
- 68071-3188_bb142d97-d227-9897-e053-2a95a90ac610
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMLODIPINE BESYLATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA077073
- Marketing category
- ANDA
- Marketing start
- 2007-09-26
- 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
- 2022-12-31
- 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 |
|---|
| 68071-3188-3 | 68071318803 | 30 TABLET in 1 BOTTLE (68071-3188-3) | 30 tablet | 2017-03-29 | 0000-00-00 | No | No | Current |
| 68071-3188-9 | 68071318809 | 90 TABLET in 1 BOTTLE (68071-3188-9) | 90 tablet | 2017-03-29 | 0000-00-00 | No | No | Current |