Lorazepam
- Product NDC
- 72789-236
- 11-digit product format
- 727890236
- Labeler code
- 72789
- Product ID
- 72789-236_40ad24fd-59cc-c810-e063-6294a90aea12
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lorazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA072926
- Marketing category
- ANDA
- Marketing start
- 2021-10-11
- 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 |
|---|
| 72789-236-30 | 72789023630 | 30 TABLET in 1 BOTTLE, PLASTIC (72789-236-30) | 30 tablet | 2022-03-09 | No | No | Historical |