amlodipine besylate
- Product NDC
- 55154-0535
- 11-digit product format
- 551540535
- Labeler code
- 55154
- Product ID
- 55154-0535_6ab295f7-c7f2-4c27-ba33-14af5e4c5a44
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- amlodipine besylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- NDA019787
- Marketing category
- NDA
- Marketing start
- 1992-07-31
- 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
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record