Product NDC: | 55154-1579 |
Proprietary Name: | Megestrol Acetate |
Non Proprietary Name: | megestrol acetate |
Active Ingredient(s): | 400 mg/10mL & nbsp; megestrol acetate |
Administration Route(s): | ORAL |
Dosage Form(s): | SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-1579 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075671 |
Marketing Category: | ANDA |
Start Marketing Date: | 20040225 |
Package NDC: | 55154-1579-5 |
Package Description: | 5 CUP, UNIT-DOSE in 1 BAG (55154-1579-5) > 10 mL in 1 CUP, UNIT-DOSE |
NDC Code | 55154-1579-5 |
Proprietary Name | Megestrol Acetate |
Package Description | 5 CUP, UNIT-DOSE in 1 BAG (55154-1579-5) > 10 mL in 1 CUP, UNIT-DOSE |
Product NDC | 55154-1579 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | megestrol acetate |
Dosage Form Name | SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20040225 |
Marketing Category Name | ANDA |
Labeler Name | Cardinal Health |
Substance Name | MEGESTROL ACETATE |
Strength Number | 400 |
Strength Unit | mg/10mL |
Pharmaceutical Classes | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC] |