Amlodipine besylate
- Product NDC
- 13668-022
- 11-digit product format
- 136680022
- Labeler code
- 13668
- Product ID
- 13668-022_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
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 13668-022-01 | 13668002201 | 100 TABLET in 1 BOTTLE (13668-022-01) | 100 tablet | 2009-02-05 | 0000-00-00 | No | No | Current |
| 13668-022-03 | 13668002203 | 300 TABLET in 1 BOTTLE (13668-022-03) | 300 tablet | 2009-02-05 | 0000-00-00 | No | No | Current |
| 13668-022-05 | 13668002205 | 500 TABLET in 1 BOTTLE (13668-022-05) | 500 tablet | 2009-02-05 | 0000-00-00 | No | No | Current |
| 13668-022-10 | 13668002210 | 1000 TABLET in 1 BOTTLE (13668-022-10) | 1000 tablet | 2009-02-05 | 0000-00-00 | No | No | Current |
| 13668-022-30 | 13668002230 | 30 TABLET in 1 BOTTLE (13668-022-30) | 30 tablet | 2009-02-05 | 0000-00-00 | No | No | Current |
| 13668-022-74 | 13668002274 | 100 TABLET in 1 CARTON (13668-022-74) | 100 tablet | 2009-02-05 | 0000-00-00 | No | No | Current |
| 13668-022-90 | 13668002290 | 90 TABLET in 1 BOTTLE (13668-022-90) | 90 tablet | 2009-02-05 | 0000-00-00 | No | No | Current |