VERAPAMIL HYDROCHLORIDE
- Product NDC
- 52584-272
- 11-digit product format
- 525840272
- Labeler code
- 52584
- Product ID
- 52584-272_22e5d801-3e07-4990-aae8-8498661431f3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- verapamil hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- General Injectables & Vaccines, Inc.
- Application
- ANDA211015
- Marketing category
- ANDA
- Marketing start
- 2019-12-03
- Marketing end
- 2023-03-31
- Substance
- VERAPAMIL HYDROCHLORIDE
- Active strength
- 3 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52584-272-01 | 52584027201 | 1 VIAL in 1 BAG (52584-272-01) > 4 mL in 1 VIAL | 1 vial | 2019-12-03 | 0000-00-00 | No | No | Current |