Midazolam Hydrochloride
- Product NDC
- 63629-2534
- 11-digit product format
- 636292534
- Labeler code
- 63629
- Product ID
- 63629-2534_e5bc4cf3-37eb-4da7-97dd-bb21d63c7a88
- 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
- Marketing end
- 0000-00-00
- Substance
- MIDAZOLAM HYDROCHLORIDE
- Active strength
- 2 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2534-1 | 63629253401 | 1 BOTTLE, GLASS in 1 CARTON (63629-2534-1) > 118 mL in 1 BOTTLE, GLASS | 2021-04-28 | 0000-00-00 | No | No | Current |