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Lorazepam
Lorazepam - 0641-6048-25 - (Lorazepam)
Drug Information of Lorazepam
| Product NDC: | 0641-6048 |
| Proprietary Name: | Lorazepam |
| Non Proprietary Name: | Lorazepam |
| Active Ingredient(s): | 2 mg/mL & nbsp; Lorazepam |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lorazepam
| Product NDC: | 0641-6048 |
| Labeler Name: | West-ward Pharmaceutical Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018140 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19800725 |
Package Information of Lorazepam
| Package NDC: | 0641-6048-25 |
| Package Description: | 25 VIAL in 1 CARTON (0641-6048-25) > 1 mL in 1 VIAL (0641-6048-01) |
NDC Information of Lorazepam
| NDC Code | 0641-6048-25 |
| Proprietary Name | Lorazepam |
| Package Description | 25 VIAL in 1 CARTON (0641-6048-25) > 1 mL in 1 VIAL (0641-6048-01) |
| Product NDC | 0641-6048 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Lorazepam |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 19800725 |
| Marketing Category Name | NDA |
| Labeler Name | West-ward Pharmaceutical Corp. |
| Substance Name | LORAZEPAM |
| Strength Number | 2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
