Flumazenil
- Product NDC
- 52584-784
- 11-digit product format
- 525840784
- Labeler code
- 52584
- Product ID
- 52584-784_bb0779bf-2803-4422-bd3e-9cb63a5ed924
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Flumazenil
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- General Injectables and Vaccines, Inc
- Application
- ANDA078527
- Marketing category
- ANDA
- Marketing start
- 2014-07-10
- Marketing end
- 2021-11-30
- Substance
- FLUMAZENIL
- Active strength
- 0 mg/mL
- Pharmacologic classes
- Benzodiazepine Antagonist [EPC]
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52584-784-01 | 52584078401 | 1 VIAL, MULTI-DOSE in 1 BAG (52584-784-01) > 5 mL in 1 VIAL, MULTI-DOSE | 2014-07-10 | 2021-11-30 | No | No | Current |