Midazolam Hydrochloride
- Product NDC
- 72162-1109
- 11-digit product format
- 721621109
- Labeler code
- 72162
- Product ID
- 72162-1109_f9324142-58b0-448d-b37d-f0f7025d02c3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Midazolam Hydrochloride
- Dosage form
- SYRUP
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076379
- Marketing category
- ANDA
- Marketing start
- 2005-05-02
- Substance
- MIDAZOLAM HYDROCHLORIDE
- Active strength
- 2 mg/mL
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| W7TTW573JJ | MIDAZOLAM HYDROCHLORIDE | 59467-96-8 | MIDAZOLAM HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1109-2 | 72162110902 | 1 BOTTLE, GLASS in 1 CARTON (72162-1109-2) / 118 mL in 1 BOTTLE, GLASS | 2023-10-25 | No | No | Historical |