Midazolam
- Product NDC
- 50090-0683
- 11-digit product format
- 500900683
- Labeler code
- 50090
- Product ID
- 50090-0683_1422b2a8-41a8-449d-8f39-604333f6a4f9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Midazolam
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- A-S Medication Solutions
- Application
- ANDA075243
- Marketing category
- ANDA
- Marketing start
- 2000-06-20
- Marketing end
- 0000-00-00
- Substance
- MIDAZOLAM HYDROCHLORIDE
- Active strength
- 5 mg/mL
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-0683-0 | 50090068300 | 10 VIAL in 1 CARTON (50090-0683-0) > 10 mL in 1 VIAL | 10 vial | 2015-10-09 | 0000-00-00 | No | No | Current |
| 50090-0683-1 | 50090068301 | 1 VIAL in 1 CARTON (50090-0683-1) > 10 mL in 1 VIAL | 1 vial | 2015-10-09 | 0000-00-00 | No | No | Current |