Verapamil Hydrochloride
- Product NDC
- 70710-1937
- 11-digit product format
- 707101937
- Labeler code
- 70710
- Product ID
- 70710-1937_9fc482f4-8fb1-47a3-a3ba-55f96fc92287
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Verapamil Hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Application
- ANDA214215
- Marketing category
- ANDA
- Marketing start
- 2023-10-17
- Substance
- VERAPAMIL HYDROCHLORIDE
- Active strength
- 2.5 mg/mL
- 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 |
|---|
| 70710-1937-7 | 70710193707 | 25 CARTON in 1 CARTON (70710-1937-7) / 5 VIAL in 1 CARTON (70710-1937-5) / 2 mL in 1 VIAL (70710-1937-1) | 25 carton | 2023-10-17 | No | No | Historical |