Product NDC: | 0054-3176 |
Proprietary Name: | Dexamethasone Intensol |
Non Proprietary Name: | Dexamethasone Intensol |
Active Ingredient(s): | 1 mg/mL & nbsp; Dexamethasone Intensol |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION, CONCENTRATE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0054-3176 |
Labeler Name: | Roxane Laboratories, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA088252 |
Marketing Category: | ANDA |
Start Marketing Date: | 19830901 |
Package NDC: | 0054-3176-44 |
Package Description: | 30 mL in 1 BOTTLE, GLASS (0054-3176-44) |
NDC Code | 0054-3176-44 |
Proprietary Name | Dexamethasone Intensol |
Package Description | 30 mL in 1 BOTTLE, GLASS (0054-3176-44) |
Product NDC | 0054-3176 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Dexamethasone Intensol |
Dosage Form Name | SOLUTION, CONCENTRATE |
Route Name | ORAL |
Start Marketing Date | 19830901 |
Marketing Category Name | ANDA |
Labeler Name | Roxane Laboratories, Inc |
Substance Name | DEXAMETHASONE |
Strength Number | 1 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |