MIDAZOLAM
- Product NDC
- 52584-749
- 11-digit product format
- 525840749
- Labeler code
- 52584
- Product ID
- 52584-749_81498f25-2a5a-45b1-9b3e-770305064cb1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- midazoalm
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- General Injectables and Vaccines, Inc.
- Application
- ANDA090850
- Marketing category
- ANDA
- Marketing start
- 2020-11-12
- Marketing end
- 2024-12-31
- Substance
- MIDAZOLAM HYDROCHLORIDE
- Active strength
- 5 mg/mL
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- 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 |
|---|
| 52584-749-01 | 52584074901 | 1 VIAL, MULTI-DOSE in 1 BAG (52584-749-01) > 10 mL in 1 VIAL, MULTI-DOSE | 2020-11-12 | 2024-12-31 | No | No | Current |