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Megestrol Acetate - 0121-4776-20 - (MEGESTROL ACETATE)

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Drug Information of Megestrol Acetate

Product NDC: 0121-4776
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: 0121-4776
Labeler Name: Pharmaceutical Associates, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076721
Marketing Category: ANDA
Start Marketing Date: 20060707

Package Information of Megestrol Acetate

Package NDC: 0121-4776-20
Package Description: 4 TRAY in 1 CASE (0121-4776-20) > 10 CUP, UNIT-DOSE in 1 TRAY > 20 mL in 1 CUP, UNIT-DOSE

NDC Information of Megestrol Acetate

NDC Code 0121-4776-20
Proprietary Name Megestrol Acetate
Package Description 4 TRAY in 1 CASE (0121-4776-20) > 10 CUP, UNIT-DOSE in 1 TRAY > 20 mL in 1 CUP, UNIT-DOSE
Product NDC 0121-4776
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name MEGESTROL ACETATE
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20060707
Marketing Category Name ANDA
Labeler Name Pharmaceutical Associates, 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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