Amlodipine Besylate
- Product NDC
- 55154-5072
- 11-digit product format
- 551545072
- Labeler code
- 55154
- Product ID
- 55154-5072_a3e72e20-95a7-4c81-8cc7-535c01b70e1f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine Besylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA076418
- Marketing category
- ANDA
- Marketing start
- 2010-01-14
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record