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Lorazepam
Lorazepam - 17478-040-01 - (Lorazepam)
Drug Information of Lorazepam
| Product NDC: | 17478-040 |
| Proprietary Name: | Lorazepam |
| Non Proprietary Name: | Lorazepam |
| Active Ingredient(s): | 2 mg/mL & nbsp; Lorazepam |
| Administration Route(s): | INTRAMUSCULAR |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lorazepam
| Product NDC: | 17478-040 |
| Labeler Name: | Akorn, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075025 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19800701 |
Package Information of Lorazepam
| Package NDC: | 17478-040-01 |
| Package Description: | 10 VIAL in 1 CARTON (17478-040-01) > 1 mL in 1 VIAL |
NDC Information of Lorazepam
| NDC Code | 17478-040-01 |
| Proprietary Name | Lorazepam |
| Package Description | 10 VIAL in 1 CARTON (17478-040-01) > 1 mL in 1 VIAL |
| Product NDC | 17478-040 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Lorazepam |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR |
| Start Marketing Date | 19800701 |
| Marketing Category Name | ANDA |
| Labeler Name | Akorn, Inc. |
| Substance Name | LORAZEPAM |
| Strength Number | 2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
