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Megestrol Acetate - 60432-126-08 - (Megestrol Acetate)

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Drug Information of Megestrol Acetate

Product NDC: 60432-126
Proprietary Name: Megestrol Acetate
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 Megestrol Acetate

Product NDC: 60432-126
Labeler Name: Morton Grove Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076721
Marketing Category: ANDA
Start Marketing Date: 20050209

Package Information of Megestrol Acetate

Package NDC: 60432-126-08
Package Description: 240 mL in 1 BOTTLE, PLASTIC (60432-126-08)

NDC Information of Megestrol Acetate

NDC Code 60432-126-08
Proprietary Name Megestrol Acetate
Package Description 240 mL in 1 BOTTLE, PLASTIC (60432-126-08)
Product NDC 60432-126
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Megestrol Acetate
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20050209
Marketing Category Name ANDA
Labeler Name Morton Grove Pharmaceuticals, Inc.
Substance Name MEGESTROL ACETATE
Strength Number 40
Strength Unit mg/mL
Pharmaceutical Classes Progesterone Congeners [Chemical/Ingredient],Progestin [EPC]

Complete Information of Megestrol Acetate


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