Lorazepam
- Product NDC
- 0409-6778
- 11-digit product format
- 004096778
- Labeler code
- 0409
- Product ID
- 0409-6778_5afe08ac-6723-4afa-81a8-697a3cc1049d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LORAZEPAM
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Hospira, Inc.
- Application
- ANDA074282
- Marketing category
- ANDA
- Marketing start
- 2018-03-06
- Marketing end
- 0000-00-00
- Substance
- LORAZEPAM
- 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
DailyMed Product Concepts#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0409-6778-02 | 00409677802 | 10 VIAL, SINGLE-DOSE in 1 CARTON (0409-6778-02) > 1 mL in 1 VIAL, SINGLE-DOSE (0409-6778-11) | 2006-01-31 | 0000-00-00 | No | No | Current |
| 0409-6778-05 | 00409677805 | 10 VIAL, SINGLE-DOSE in 1 CARTON (0409-6778-05) > 1 mL in 1 VIAL, SINGLE-DOSE (0409-6778-15) | 2018-03-06 | 0000-00-00 | No | No | Current |