Verapamil Hydrochloride
- Product NDC
- 52584-271
- 11-digit product format
- 525840271
- Labeler code
- 52584
- Product ID
- 52584-271_75a3a7bc-cc4f-4997-8ff5-a2c9a71d1082
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Verapamil Hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- General Injectables and Vaccines, Inc.
- Application
- ANDA211015
- Marketing category
- ANDA
- Marketing start
- 2019-07-09
- Marketing end
- 0000-00-00
- Substance
- VERAPAMIL HYDROCHLORIDE
- Active strength
- 3 mg/mL
- 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 |
|---|
| 52584-271-01 | 52584027101 | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-271-01) > 2 mL in 1 VIAL, SINGLE-DOSE | 2019-07-09 | 0000-00-00 | No | No | Current |