Lorazepam
- Product NDC
- 71335-1311
- 11-digit product format
- 713351311
- Labeler code
- 71335
- Product ID
- 71335-1311_26d9a35d-15e4-4d88-ae57-11a0c3432dde
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lorazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA203572
- Marketing category
- ANDA
- Marketing start
- 2017-03-24
- Marketing end
- 0000-00-00
- Substance
- LORAZEPAM
- Active strength
- 1 mg/1
- 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 |
|---|
| 71335-1311-1 | 71335131101 | 30 TABLET in 1 BOTTLE (71335-1311-1) | 30 tablet | 2019-08-26 | 0000-00-00 | No | No | Current |