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Megestrol Acetate - 51079-434-20 - (Megestrol Acetate)

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Drug Information of Megestrol Acetate

Product NDC: 51079-434
Proprietary Name: Megestrol Acetate
Non Proprietary Name: Megestrol Acetate
Active Ingredient(s): 20    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: 51079-434
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: 51079-434-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-434-20) > 1 TABLET in 1 BLISTER PACK (51079-434-01)

NDC Information of Megestrol Acetate

NDC Code 51079-434-20
Proprietary Name Megestrol Acetate
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-434-20) > 1 TABLET in 1 BLISTER PACK (51079-434-01)
Product NDC 51079-434
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 20
Strength Unit mg/1
Pharmaceutical Classes Progesterone Congeners [Chemical/Ingredient],Progestin [EPC]

Complete Information of Megestrol Acetate


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