Product NDC: | 68094-528 |
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: | 68094-528 |
Labeler Name: | Precision Dose Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075671 |
Marketing Category: | ANDA |
Start Marketing Date: | 20040225 |
Package NDC: | 68094-528-62 |
Package Description: | 3 TRAY in 1 CASE (68094-528-62) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (68094-528-59) |
NDC Code | 68094-528-62 |
Proprietary Name | Megestrol Acetate |
Package Description | 3 TRAY in 1 CASE (68094-528-62) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (68094-528-59) |
Product NDC | 68094-528 |
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 | Precision Dose Inc. |
Substance Name | MEGESTROL ACETATE |
Strength Number | 400 |
Strength Unit | mg/10mL |
Pharmaceutical Classes | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC] |