Product NDC: | 0121-0770 |
Proprietary Name: | Lorazepam |
Non Proprietary Name: | Lorazepam |
Active Ingredient(s): | 2 mg/mL & nbsp; Lorazepam |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0121-0770 |
Labeler Name: | Pharmaceutical Associates, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA090260 |
Marketing Category: | ANDA |
Start Marketing Date: | 20101101 |
Package NDC: | 0121-0770-01 |
Package Description: | 30 mL in 1 BOTTLE, DROPPER (0121-0770-01) |
NDC Code | 0121-0770-01 |
Proprietary Name | Lorazepam |
Package Description | 30 mL in 1 BOTTLE, DROPPER (0121-0770-01) |
Product NDC | 0121-0770 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Lorazepam |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20101101 |
Marketing Category Name | ANDA |
Labeler Name | Pharmaceutical Associates, Inc. |
Substance Name | LORAZEPAM |
Strength Number | 2 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |