Midazolam
- Product NDC
- 65293-411
- 11-digit product format
- 652930411
- Labeler code
- 65293
- Product ID
- 65293-411_99d569d6-86b7-560b-e053-2a95a90a0780
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- MIDAZOLAM HYDROCHLORIDE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- The Medicines Company
- Application
- ANDA075154
- Marketing category
- ANDA
- Marketing start
- 2000-07-14
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record