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Megace ES
Megace ES - 49884-949-69 - (megesterol acetate)
Drug Information of Megace ES
| Product NDC: | 49884-949 |
| 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: | 49884-949 |
| Labeler Name: | Par Pharmaceutical, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021778 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20050702 |
Package Information of Megace ES
| Package NDC: | 49884-949-69 |
| Package Description: | 150 mL in 1 BOTTLE (49884-949-69) |
NDC Information of Megace ES
| NDC Code | 49884-949-69 |
| Proprietary Name | Megace ES |
| Package Description | 150 mL in 1 BOTTLE (49884-949-69) |
| Product NDC | 49884-949 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | megesterol acetate |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20050702 |
| Marketing Category Name | NDA |
| Labeler Name | Par Pharmaceutical, Inc |
| Substance Name | MEGESTROL ACETATE |
| Strength Number | 125 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC] |
