VERAPAMIL HYDROCHLORIDE
- Product NDC
- 72162-2232
- 11-digit product format
- 721622232
- Labeler code
- 72162
- Product ID
- 72162-2232_d10e4b7e-6e14-40a5-9bd3-94e51e4515b8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- VERAPAMIL HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA071881
- Marketing category
- ANDA
- Marketing start
- 2011-01-07
- Substance
- VERAPAMIL HYDROCHLORIDE
- Active strength
- 80 mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| V3888OEY5R | VERAPAMIL HYDROCHLORIDE | 152-11-4 | VERAPAMIL HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2232-1 | 72162223201 | 100 TABLET in 1 BOTTLE (72162-2232-1) | 100 tablet | 2024-01-26 | No | No | Historical |