Amlodipine besylate
- Product NDC
- 59115-057
- 11-digit product format
- 591150057
- Labeler code
- 59115
- Product ID
- 59115-057_1e1780ca-5513-49a7-9ee3-f27be5b2ccce
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine besylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Hikma Pharmaceutical
- Application
- ANDA077771
- Marketing category
- ANDA
- Marketing start
- 2011-04-12
- 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
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record