verapamil hydrochloride
- Product NDC
- 68071-3072
- 11-digit product format
- 680713072
- Labeler code
- 68071
- Product ID
- 68071-3072_bb12e55b-3bc2-f4c8-e053-2a95a90a2a1c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- verapamil hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-3072-3 | 68071307203 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68071-3072-3) | 2017-03-14 | 0000-00-00 | No | No | Current |
| 68071-3072-6 | 68071307206 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68071-3072-6) | 2017-03-14 | 0000-00-00 | No | No | Current |
| 68071-3072-9 | 68071307209 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68071-3072-9) | 2017-03-14 | 0000-00-00 | No | No | Current |