Midazolam Hydrochloride
- Product NDC
- 0904-7114
- 11-digit product format
- 009047114
- Labeler code
- 0904
- Product ID
- 0904-7114_2a9d7bfe-a757-4c5a-849d-b5ae1d2033e4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Midazolam Hydrochloride
- Dosage form
- SYRUP
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA075873
- Marketing category
- ANDA
- Marketing start
- 2002-04-30
- 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
- 2022-12-31
- 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 |
|---|
| 0904-7114-22 | 00904711422 | 30 CUP, UNIT-DOSE in 1 CASE (0904-7114-22) > 2.5 mL in 1 CUP, UNIT-DOSE (0904-7114-12) | 2002-04-30 | 0000-00-00 | No | No | Current |