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MEGESTROL ACETATE - 54868-5389-1 - (megestrol acetate)

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Drug Information of MEGESTROL ACETATE

Product NDC: 54868-5389
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: 54868-5389
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075671
Marketing Category: ANDA
Start Marketing Date: 20050901

Package Information of MEGESTROL ACETATE

Package NDC: 54868-5389-1
Package Description: 480 mL in 1 BOTTLE, PLASTIC (54868-5389-1)

NDC Information of MEGESTROL ACETATE

NDC Code 54868-5389-1
Proprietary Name MEGESTROL ACETATE
Package Description 480 mL in 1 BOTTLE, PLASTIC (54868-5389-1)
Product NDC 54868-5389
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name megestrol acetate
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20050901
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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


General Information