Midazolam
- Product NDC
- 0404-9912
- 11-digit product format
- 004049912
- Labeler code
- 0404
- Product ID
- 0404-9912_445f7470-be78-446f-80db-b239ee38d33e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Midazolam
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Henry Schein, Inc.
- Application
- ANDA075154
- Marketing category
- ANDA
- Marketing start
- 2022-01-13
- Marketing end
- 0000-00-00
- Substance
- MIDAZOLAM HYDROCHLORIDE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0404-9912-10 | 00404991210 | 1 VIAL in 1 BAG (0404-9912-10) > 10 mL in 1 VIAL | 1 vial | 2022-01-13 | 0000-00-00 | No | No | Current |