Verapamil Hydrochloride
- Product NDC
- 66267-294
- 11-digit product format
- 662670294
- Labeler code
- 66267
- Product ID
- 66267-294_9cbe1f2d-6747-fb5e-e053-2a95a90ae790
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Verapamil Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA071881
- Marketing category
- ANDA
- Marketing start
- 2011-01-07
- Marketing end
- 0000-00-00
- Substance
- VERAPAMIL HYDROCHLORIDE
- Active strength
- 120 mg/1
- Pharmacologic classes
- P-Glycoprotein Inhibitors [MoA],Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 3A Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 66267-294-90 | 66267029490 | 90 TABLET in 1 BOTTLE (66267-294-90) | 90 tablet | 2016-11-09 | 0000-00-00 | No | No | Current |