VERAPAMIL HYDROCHLORIDE
- Product NDC
- 70518-2184
- 11-digit product format
- 705182184
- Labeler code
- 70518
- Product ID
- 70518-2184_d7ff0cc9-d731-655f-e053-2a95a90ad977
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- VERAPAMIL HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA071881
- Marketing category
- ANDA
- Marketing start
- 2019-07-02
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2184-1 | 70518218401 | 100 CUP, UNIT-DOSE in 1 BOX (70518-2184-1) > 1 TABLET in 1 CUP, UNIT-DOSE (70518-2184-2) | 2022-01-26 | 0000-00-00 | No | No | Current |