| Product NDC: | 0187-0063 |
| Proprietary Name: | Ativan |
| Non Proprietary Name: | lorazepam |
| Active Ingredient(s): | .5 mg/1 & nbsp; lorazepam |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0187-0063 |
| Labeler Name: | Valeant Pharmaceuticals North America LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017794 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130501 |
| Package NDC: | 0187-0063-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (0187-0063-01) |
| NDC Code | 0187-0063-01 |
| Proprietary Name | Ativan |
| Package Description | 100 TABLET in 1 BOTTLE (0187-0063-01) |
| Product NDC | 0187-0063 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | lorazepam |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130501 |
| Marketing Category Name | NDA |
| Labeler Name | Valeant Pharmaceuticals North America LLC |
| Substance Name | LORAZEPAM |
| Strength Number | .5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |