Product NDC: | 0054-3185 |
Proprietary Name: | Diazepam Intensol |
Non Proprietary Name: | Diazepam Intensol |
Active Ingredient(s): | 5 mg/mL & nbsp; Diazepam Intensol |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION, CONCENTRATE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0054-3185 |
Labeler Name: | Roxane Laboratories, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA071415 |
Marketing Category: | ANDA |
Start Marketing Date: | 19870403 |
Package NDC: | 0054-3185-44 |
Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (0054-3185-44) > 30 mL in 1 BOTTLE, DROPPER |
NDC Code | 0054-3185-44 |
Proprietary Name | Diazepam Intensol |
Package Description | 1 BOTTLE, DROPPER in 1 CARTON (0054-3185-44) > 30 mL in 1 BOTTLE, DROPPER |
Product NDC | 0054-3185 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Diazepam Intensol |
Dosage Form Name | SOLUTION, CONCENTRATE |
Route Name | ORAL |
Start Marketing Date | 19870403 |
Marketing Category Name | ANDA |
Labeler Name | Roxane Laboratories, Inc |
Substance Name | DIAZEPAM |
Strength Number | 5 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |