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Megestrol Acetate
Megestrol Acetate - 51079-435-20 - (Megestrol Acetate)
Drug Information of Megestrol Acetate
| Product NDC: | 51079-435 |
| Proprietary Name: | Megestrol Acetate |
| Non Proprietary Name: | Megestrol Acetate |
| Active Ingredient(s): | 40 mg/1 & nbsp; Megestrol Acetate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Megestrol Acetate
| Product NDC: | 51079-435 |
| Labeler Name: | UDL Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074621 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110513 |
Package Information of Megestrol Acetate
| Package NDC: | 51079-435-20 |
| Package Description: | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-435-20) > 1 TABLET in 1 BLISTER PACK (51079-435-01) |
NDC Information of Megestrol Acetate
| NDC Code | 51079-435-20 |
| Proprietary Name | Megestrol Acetate |
| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-435-20) > 1 TABLET in 1 BLISTER PACK (51079-435-01) |
| Product NDC | 51079-435 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Megestrol Acetate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110513 |
| Marketing Category Name | ANDA |
| Labeler Name | UDL Laboratories, Inc. |
| Substance Name | MEGESTROL ACETATE |
| Strength Number | 40 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC] |
