VERAPAMIL HYDROCHLORIDE
- Product NDC
- 70518-1464
- 11-digit product format
- 705181464
- Labeler code
- 70518
- Product ID
- 70518-1464_e43c1093-0b9c-30c7-e053-2a95a90a9f96
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- VERAPAMIL HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA071881
- Marketing category
- ANDA
- Marketing start
- 2018-10-04
- Marketing end
- 0000-00-00
- Substance
- VERAPAMIL HYDROCHLORIDE
- Active strength
- 120 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 |
|---|
| 70518-1464-0 | 70518146400 | 30 TABLET in 1 BLISTER PACK (70518-1464-0) | 30 tablet | 2018-10-04 | 0000-00-00 | No | No | Current |