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Lorazepam
Lorazepam - 50383-705-30 - (Lorazepam)
Drug Information of Lorazepam
| Product NDC: | 50383-705 |
| Proprietary Name: | Lorazepam |
| Non Proprietary Name: | Lorazepam |
| Active Ingredient(s): | 2 mg/mL & nbsp; Lorazepam |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CONCENTRATE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lorazepam
| Product NDC: | 50383-705 |
| Labeler Name: | Hi-Tech Pharmacal Co., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA200169 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120130 |
Package Information of Lorazepam
| Package NDC: | 50383-705-30 |
| Package Description: | 1 BOTTLE in 1 CARTON (50383-705-30) > 30 mL in 1 BOTTLE |
NDC Information of Lorazepam
| NDC Code | 50383-705-30 |
| Proprietary Name | Lorazepam |
| Package Description | 1 BOTTLE in 1 CARTON (50383-705-30) > 30 mL in 1 BOTTLE |
| Product NDC | 50383-705 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Lorazepam |
| Dosage Form Name | CONCENTRATE |
| Route Name | ORAL |
| Start Marketing Date | 20120130 |
| Marketing Category Name | ANDA |
| Labeler Name | Hi-Tech Pharmacal Co., Inc. |
| Substance Name | LORAZEPAM |
| Strength Number | 2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
