Product NDC: | 60432-466 |
Proprietary Name: | Dexamethasone |
Non Proprietary Name: | Dexamethasone |
Active Ingredient(s): | .5 mg/5mL & nbsp; Dexamethasone |
Administration Route(s): | ORAL |
Dosage Form(s): | ELIXIR |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 60432-466 |
Labeler Name: | Morton Grove Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA088254 |
Marketing Category: | ANDA |
Start Marketing Date: | 19830727 |
Package NDC: | 60432-466-08 |
Package Description: | 1 BOTTLE, GLASS in 1 BOX (60432-466-08) > 237 mL in 1 BOTTLE, GLASS |
NDC Code | 60432-466-08 |
Proprietary Name | Dexamethasone |
Package Description | 1 BOTTLE, GLASS in 1 BOX (60432-466-08) > 237 mL in 1 BOTTLE, GLASS |
Product NDC | 60432-466 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Dexamethasone |
Dosage Form Name | ELIXIR |
Route Name | ORAL |
Start Marketing Date | 19830727 |
Marketing Category Name | ANDA |
Labeler Name | Morton Grove Pharmaceuticals, Inc. |
Substance Name | DEXAMETHASONE |
Strength Number | .5 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |