Lorazepam
- Product NDC
- 68071-3751
- 11-digit product format
- 680713751
- Labeler code
- 68071
- Product ID
- 68071-3751_29f63525-283a-946c-e063-6294a90aebb1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lorazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA076045
- Marketing category
- ANDA
- Marketing start
- 2023-06-25
- Substance
- LORAZEPAM
- Active strength
- .5 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 |
|---|
| 68071-3751-6 | 68071375106 | 60 TABLET in 1 BOTTLE (68071-3751-6) | 60 tablet | 2024-12-23 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Lorazepam Tablets, USP CIV | NuCare Pharmaceuticals, Inc. | 2024-12-23 | HUMAN PRESCRIPTION DRUG LABEL | 1 |