VERAPAMIL HYDROCHLORIDE
- Product NDC
- 70518-3533
- 11-digit product format
- 705183533
- Labeler code
- 70518
- Product ID
- 70518-3533_e9954191-cb73-4ed5-e053-2995a90aef4b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- VERAPAMIL HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA206173
- Marketing category
- ANDA
- Marketing start
- 2022-09-23
- Marketing end
- 0000-00-00
- Substance
- VERAPAMIL HYDROCHLORIDE
- Active strength
- 240 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
- 2023-12-31
- 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 |
|---|
| 70518-3533-0 | 70518353300 | 100 POUCH in 1 BOX (70518-3533-0) > 1 TABLET in 1 POUCH (70518-3533-1) | 100 pouch | 2022-09-23 | 0000-00-00 | No | No | Current |