Lorazepam
- Product NDC
- 68071-5137
- 11-digit product format
- 680715137
- Labeler code
- 68071
- Product ID
- 68071-5137_bbf52b65-38c9-9c35-e053-2995a90a04f2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lorazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA072926
- Marketing category
- ANDA
- Marketing start
- 1991-10-31
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| O26FZP769L | LORAZEPAM | 846-49-1 | LORAZEPAM |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-5137-4 | 68071513704 | 4 TABLET in 1 BOTTLE (68071-5137-4) | 4 tablet | 2019-12-17 | 0000-00-00 | No | No | Current |