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Lorazepam
Lorazepam - 21695-239-03 - (Lorazepam)
Drug Information of Lorazepam
| Product NDC: | 21695-239 |
| 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: | 21695-239 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA071194 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19880415 |
Package Information of Lorazepam
| Package NDC: | 21695-239-03 |
| Package Description: | 3 TABLET in 1 BOTTLE (21695-239-03) |
NDC Information of Lorazepam
| NDC Code | 21695-239-03 |
| Proprietary Name | Lorazepam |
| Package Description | 3 TABLET in 1 BOTTLE (21695-239-03) |
| Product NDC | 21695-239 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Lorazepam |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19880415 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | LORAZEPAM |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
