Amlodipine Besylate
- Product NDC
- 0615-8199
- 11-digit product format
- 006158199
- Labeler code
- 0615
- Product ID
- 0615-8199_3bd86769-1b9e-42fd-ab9c-1c67297952bb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine Besylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA203245
- Marketing category
- ANDA
- Marketing start
- 2014-03-03
- Marketing end
- 2020-09-30
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record