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LORAZEPAM
LORAZEPAM - 42549-655-10 - (LORAZEPAM)
Drug Information of LORAZEPAM
| Product NDC: | 42549-655 |
| Proprietary Name: | LORAZEPAM |
| Non Proprietary Name: | LORAZEPAM |
| Active Ingredient(s): | 1 mg/1 & nbsp; LORAZEPAM |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LORAZEPAM
| Product NDC: | 42549-655 |
| Labeler Name: | STAT Rx USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA072927 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19911031 |
Package Information of LORAZEPAM
| Package NDC: | 42549-655-10 |
| Package Description: | 10 TABLET in 1 BOTTLE (42549-655-10) |
NDC Information of LORAZEPAM
| NDC Code | 42549-655-10 |
| Proprietary Name | LORAZEPAM |
| Package Description | 10 TABLET in 1 BOTTLE (42549-655-10) |
| Product NDC | 42549-655 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | LORAZEPAM |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19911031 |
| Marketing Category Name | ANDA |
| Labeler Name | STAT Rx USA LLC |
| Substance Name | LORAZEPAM |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
