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MEGACE ES
MEGACE ES - 54868-5572-0 - (megesterol acetate)
Drug Information of MEGACE ES
| Product NDC: | 54868-5572 |
| Proprietary Name: | MEGACE ES |
| Non Proprietary Name: | megesterol acetate |
| Active Ingredient(s): | 125 mg/mL & nbsp; megesterol acetate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MEGACE ES
| Product NDC: | 54868-5572 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021778 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20060413 |
Package Information of MEGACE ES
| Package NDC: | 54868-5572-0 |
| Package Description: | 150 mL in 1 BOTTLE (54868-5572-0) |
NDC Information of MEGACE ES
| NDC Code | 54868-5572-0 |
| Proprietary Name | MEGACE ES |
| Package Description | 150 mL in 1 BOTTLE (54868-5572-0) |
| Product NDC | 54868-5572 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | megesterol acetate |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20060413 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | MEGESTROL ACETATE |
| Strength Number | 125 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC] |
