Verapamil Hydrochloride
- Product NDC
- 51079-899
- 11-digit product format
- 510790899
- Labeler code
- 51079
- Product ID
- 51079-899_7d8f163b-f290-42cc-e053-2991aa0aef2f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- verapamil hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA074587
- Marketing category
- ANDA
- Marketing start
- 1998-11-15
- Marketing end
- 0000-00-00
- Substance
- VERAPAMIL HYDROCHLORIDE
- Active strength
- 180 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
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record