Verapamil Hydrochloride
- Product NDC
- 71335-2087
- 11-digit product format
- 713352087
- Labeler code
- 71335
- Product ID
- 71335-2087_aa812d96-3c8c-4cdf-b31d-5674cfa5c8c5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Verapamil Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA072924
- Marketing category
- ANDA
- Marketing start
- 1993-06-29
- Substance
- VERAPAMIL HYDROCHLORIDE
- Active strength
- 40 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 | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2087-1 | 71335208701 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2087-1) | 2022-05-16 | No | No | Historical |