Product NDC: | 0054-8207 |
Proprietary Name: | Diazepam |
Non Proprietary Name: | Diazepam |
Active Ingredient(s): | 5 mg/5mL & nbsp; Diazepam |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0054-8207 |
Labeler Name: | Roxane Laboratories, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA070928 |
Marketing Category: | ANDA |
Start Marketing Date: | 19900614 |
Package NDC: | 0054-8207-16 |
Package Description: | 4 TRAY in 1 CARTON (0054-8207-16) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE |
NDC Code | 0054-8207-16 |
Proprietary Name | Diazepam |
Package Description | 4 TRAY in 1 CARTON (0054-8207-16) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE |
Product NDC | 0054-8207 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Diazepam |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 19900614 |
Marketing Category Name | ANDA |
Labeler Name | Roxane Laboratories, Inc |
Substance Name | DIAZEPAM |
Strength Number | 5 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |