Verapamil Hydrochloride
- Product NDC
- 0093-3043
- 11-digit product format
- 000933043
- Labeler code
- 0093
- Product ID
- 0093-3043_dfa87de0-b5a5-45d8-af05-76bcb35e2123
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- verapamil hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA Inc
- Application
- ANDA074587
- Marketing category
- ANDA
- Marketing start
- 2014-03-10
- Marketing end
- 2019-12-31
- Substance
- VERAPAMIL HYDROCHLORIDE
- Active strength
- 120 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record