AMLODIPINE BESYLATE
- Product NDC
- 68071-1974
- 11-digit product format
- 680711974
- Labeler code
- 68071
- Product ID
- 68071-1974_bc05d708-7e9c-c871-e053-2995a90afead
- 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
- 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
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 |
|---|
| 68071-1974-3 | 68071197403 | 30 TABLET in 1 BOTTLE (68071-1974-3) | 30 tablet | 2017-02-22 | 0000-00-00 | No | No | Current |
| 68071-1974-6 | 68071197406 | 60 TABLET in 1 BOTTLE (68071-1974-6) | 60 tablet | 2017-02-22 | 0000-00-00 | No | No | Current |
| 68071-1974-9 | 68071197409 | 90 TABLET in 1 BOTTLE (68071-1974-9) | 90 tablet | 2017-02-22 | 0000-00-00 | No | No | Current |