verapamil hydrochloride
- Product NDC
- 71335-0041
- 11-digit product format
- 713350041
- Labeler code
- 71335
- Product ID
- 71335-0041_fc558da1-2d5b-4479-ac22-bf02979842c1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- verapamil hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090700
- Marketing category
- ANDA
- Marketing start
- 2011-08-05
- Marketing end
- 0000-00-00
- Substance
- VERAPAMIL HYDROCHLORIDE
- Active strength
- 180 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0041-1 | 71335004101 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0041-1) | 2017-10-27 | 0000-00-00 | No | No | Current |
| 71335-0041-2 | 71335004102 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0041-2) | 2017-10-27 | 0000-00-00 | No | No | Current |
| 71335-0041-3 | 71335004103 | 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0041-3) | 2017-10-27 | 0000-00-00 | No | No | Current |