Verapamil Hydrochloride
- Product NDC
- 0904-2920
- 11-digit product format
- 009042920
- Labeler code
- 0904
- Product ID
- 0904-2920_c2d2b8e3-76ee-4a0f-962f-11e20950190b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Verapamil Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA070995
- Marketing category
- ANDA
- Marketing start
- 1986-10-01
- Marketing end
- 2022-08-31
- 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
- 0000-00-00
- 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 |
|---|
| 0904-2920-61 | 00904292061 | 100 BLISTER PACK in 1 CARTON (0904-2920-61) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 100 blister pack | 1986-10-01 | 0000-00-00 | No | No | Current |