Lorazepam
- Product NDC
- 60687-831
- 11-digit product format
- 606870831
- Labeler code
- 60687
- Product ID
- 60687-831_1f0a358c-b2ef-1088-e063-6394a90add6d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lorazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA203572
- Marketing category
- ANDA
- Marketing start
- 2025-09-14
- Substance
- LORAZEPAM
- Active strength
- 1 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 60687-831-01 | 60687083101 | 100 BLISTER PACK in 1 CARTON (60687-831-01) / 1 TABLET in 1 BLISTER PACK (60687-831-11) | 100 blister pack | 2025-09-14 | No | No | Historical |