Flumazenil
- Product NDC
- 70518-3456
- 11-digit product format
- 705183456
- Labeler code
- 70518
- Product ID
- 70518-3456_ec552c22-0386-b399-e053-2a95a90a792f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FLUMAZENIL
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076955
- Marketing category
- ANDA
- Marketing start
- 2021-07-21
- Marketing end
- 0000-00-00
- Substance
- FLUMAZENIL
- Active strength
- 0 mg/mL
- Pharmacologic classes
- Benzodiazepine Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 70518-3456-0 | 70518345600 | 10 VIAL, MULTI-DOSE in 1 TRAY (70518-3456-0) > 5 mL in 1 VIAL, MULTI-DOSE | 2021-07-21 | 0000-00-00 | No | No | Current |