Amlodipine besylate
- Product NDC
- 0143-9961
- 11-digit product format
- 001439961
- Labeler code
- 0143
- Product ID
- 0143-9961_2f566e71-af88-4b65-9f60-14096dba2b67
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine besylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Application
- ANDA077771
- Marketing category
- ANDA
- Marketing start
- 2011-04-12
- 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
- 2021-12-31
- 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 |
|---|
| 0143-9961-01 | 00143996101 | 100 TABLET in 1 BOTTLE (0143-9961-01) | 100 tablet | 2011-04-12 | 0000-00-00 | No | No | Current |
| 0143-9961-09 | 00143996109 | 90 TABLET in 1 BOTTLE (0143-9961-09) | 90 tablet | 2011-04-12 | 0000-00-00 | No | No | Current |
| 0143-9961-30 | 00143996130 | 30 TABLET in 1 BOTTLE (0143-9961-30) | 30 tablet | 2011-04-12 | 0000-00-00 | No | No | Current |