Amlodipine besylate
- Product NDC
- 13668-024
- 11-digit product format
- 136680024
- Labeler code
- 13668
- Product ID
- 13668-024_ba0da07a-107e-2c66-e053-2995a90ab96a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine besylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Torrent Pharmaceuticals Limited
- Application
- ANDA078573
- Marketing category
- ANDA
- Marketing start
- 2009-02-05
- 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
- 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 |
|---|
| 13668-024-01 | 13668002401 | 100 TABLET in 1 BOTTLE (13668-024-01) | 100 tablet | 2009-02-05 | 0000-00-00 | No | No | Current |
| 13668-024-03 | 13668002403 | 300 TABLET in 1 BOTTLE (13668-024-03) | 300 tablet | 2009-02-05 | 0000-00-00 | No | No | Current |
| 13668-024-05 | 13668002405 | 500 TABLET in 1 BOTTLE (13668-024-05) | 500 tablet | 2009-02-05 | 0000-00-00 | No | No | Current |
| 13668-024-10 | 13668002410 | 1000 TABLET in 1 BOTTLE (13668-024-10) | 1000 tablet | 2009-02-05 | 0000-00-00 | No | No | Current |
| 13668-024-20 | 13668002420 | 2000 TABLET in 1 BOTTLE (13668-024-20) | 2000 tablet | 2009-02-05 | 0000-00-00 | No | No | Current |
| 13668-024-30 | 13668002430 | 30 TABLET in 1 BOTTLE (13668-024-30) | 30 tablet | 2009-02-05 | 0000-00-00 | No | No | Current |
| 13668-024-74 | 13668002474 | 100 TABLET in 1 CARTON (13668-024-74) | 100 tablet | 2009-02-05 | 0000-00-00 | No | No | Current |
| 13668-024-90 | 13668002490 | 90 TABLET in 1 BOTTLE (13668-024-90) | 90 tablet | 2009-02-05 | 0000-00-00 | No | No | Current |