Product NDC: | 49999-059 |
Proprietary Name: | Dexamethasone |
Non Proprietary Name: | Dexamethasone |
Active Ingredient(s): | 4 mg/1 & nbsp; Dexamethasone |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49999-059 |
Labeler Name: | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA084612 |
Marketing Category: | ANDA |
Start Marketing Date: | 19780719 |
Package NDC: | 49999-059-60 |
Package Description: | 60 TABLET in 1 BOTTLE, PLASTIC (49999-059-60) |
NDC Code | 49999-059-60 |
Proprietary Name | Dexamethasone |
Package Description | 60 TABLET in 1 BOTTLE, PLASTIC (49999-059-60) |
Product NDC | 49999-059 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Dexamethasone |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19780719 |
Marketing Category Name | ANDA |
Labeler Name | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Substance Name | DEXAMETHASONE |
Strength Number | 4 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |