Midazolam Hydrochloride
- Product NDC
- 0409-2307
- 11-digit product format
- 004092307
- Labeler code
- 0409
- Product ID
- 0409-2307_a0eebbe6-d3ca-473b-9683-4f4f4b266373
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- MIDAZOLAM HYDROCHLORIDE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Hospira, Inc.
- Application
- ANDA075856
- Marketing category
- ANDA
- Marketing start
- 2005-05-03
- 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
- 2021-12-31
- 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 |
|---|
| 0409-2307-60 | 00409230760 | 10 CARTRIDGE in 1 CARTON (0409-2307-60) > 1 mL in 1 CARTRIDGE (0409-2307-03) | 10 cartridge | 2005-05-03 | 0000-00-00 | No | No | Current |