amlodipine besylate
- Product NDC
- 0832-0042
- 11-digit product format
- 008320042
- Labeler code
- 0832
- Product ID
- 0832-0042_0ebe12ae-5916-46cb-9193-dd3ca061643f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- amlodipine besylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Upsher-Smith Laboratories, LLC
- Application
- ANDA077759
- Marketing category
- ANDA
- Marketing start
- 2007-07-09
- 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
- 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 |
|---|
| 0832-0042-01 | 00832004201 | 10 BLISTER PACK in 1 CARTON (0832-0042-01) > 10 TABLET in 1 BLISTER PACK (0832-0042-89) | 10 blister pack | 2007-07-09 | 0000-00-00 | No | No | Current |
| 0832-0042-09 | 00832004209 | 90 TABLET in 1 BOTTLE (0832-0042-09) | 90 tablet | 2007-07-09 | 0000-00-00 | No | No | Current |
| 0832-0042-10 | 00832004210 | 1000 TABLET in 1 BOTTLE (0832-0042-10) | 1000 tablet | 2007-07-09 | 0000-00-00 | No | No | Current |