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MEGACE
MEGACE - 0015-0508-42 - (MEGESTROL ACETATE)
Drug Information of MEGACE
| Product NDC: | 0015-0508 |
| Proprietary Name: | MEGACE |
| 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 MEGACE
| Product NDC: | 0015-0508 |
| Labeler Name: | E.R. Squibb & Sons, L.L.C. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020264 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090601 |
Package Information of MEGACE
| Package NDC: | 0015-0508-42 |
| Package Description: | 1 BOTTLE in 1 CARTON (0015-0508-42) > 240 mL in 1 BOTTLE |
NDC Information of MEGACE
| NDC Code | 0015-0508-42 |
| Proprietary Name | MEGACE |
| Package Description | 1 BOTTLE in 1 CARTON (0015-0508-42) > 240 mL in 1 BOTTLE |
| Product NDC | 0015-0508 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | MEGESTROL ACETATE |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20090601 |
| Marketing Category Name | NDA |
| Labeler Name | E.R. Squibb & Sons, L.L.C. |
| Substance Name | MEGESTROL ACETATE |
| Strength Number | 40 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC] |
