Verapamil Hydrochloride
- Product NDC
- 63629-8017
- 11-digit product format
- 636298017
- Labeler code
- 63629
- Product ID
- 63629-8017_229acbe7-a2a3-4703-8b72-af1fb79d63e2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Verapamil Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA020943
- Marketing category
- NDA
- Marketing start
- 1998-11-25
- Marketing end
- 0000-00-00
- Substance
- VERAPAMIL HYDROCHLORIDE
- Active strength
- 100 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
- 2020-12-31
- 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 |
|---|
| 63629-8017-1 | 63629801701 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-8017-1) | 2019-07-26 | 0000-00-00 | No | No | Current |