| 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] |