Verapamil Hydrochloride
- Product NDC
- 63629-4353
- 11-digit product format
- 636294353
- Labeler code
- 63629
- Product ID
- 63629-4353_9a4567b7-65d9-4017-9075-4378e4b8de4c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- verapamil hydrochloride
- Dosage form
- CAPSULE, DELAYED RELEASE PELLETS
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA019614
- Marketing category
- NDA
- Marketing start
- 1990-05-29
- Marketing end
- 0000-00-00
- Substance
- VERAPAMIL HYDROCHLORIDE
- Active strength
- 360 mg/1
- Pharmacologic classes
- P-Glycoprotein Inhibitors [MoA],Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 3A Inhibitors [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#