midazolam
- Product NDC
- 72611-741
- 11-digit product format
- 726110741
- Labeler code
- 72611
- Product ID
- 72611-741_dcba4284-fbc8-98e8-3143-690015472880
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- midazolam
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Almaject, Inc.
- Application
- ANDA090696
- Marketing category
- ANDA
- Marketing start
- 2020-04-14
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72611-741 | MIDAZOLAM INJECTION, SOLUTION [ALMAJECT, INC.] | 5 | Legacy NDC | 20241020_c33919da-1d84-ed01-a5e5-62330407336e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72611-741-25 | 72611074125 | 25 VIAL, SINGLE-DOSE in 1 CARTON (72611-741-25) > 2 mL in 1 VIAL, SINGLE-DOSE (72611-741-01) | 2020-04-14 | 0000-00-00 | No | No | Current |