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Megestrol Acetate
Megestrol Acetate - 66689-020-50 - (Megestrol Acetate)
Drug Information of Megestrol Acetate
| Product NDC: | 66689-020 |
| Proprietary Name: | Megestrol Acetate |
| Non Proprietary Name: | Megestrol Acetate |
| Active Ingredient(s): | 40 mg/mL & nbsp; Megestrol Acetate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Megestrol Acetate
| Product NDC: | 66689-020 |
| Labeler Name: | VistaPharm, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075671 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120822 |
Package Information of Megestrol Acetate
| Package NDC: | 66689-020-50 |
| Package Description: | 5 TRAY in 1 CASE (66689-020-50) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (66689-020-01) |
NDC Information of Megestrol Acetate
| NDC Code | 66689-020-50 |
| Proprietary Name | Megestrol Acetate |
| Package Description | 5 TRAY in 1 CASE (66689-020-50) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (66689-020-01) |
| Product NDC | 66689-020 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Megestrol Acetate |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20120822 |
| Marketing Category Name | ANDA |
| Labeler Name | VistaPharm, Inc. |
| Substance Name | MEGESTROL ACETATE |
| Strength Number | 40 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC] |
