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Megestrol Acetate - 68094-518-61 - (Megestrol Acetate)

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Drug Information of Megestrol Acetate

Product NDC: 68094-518
Proprietary Name: Megestrol Acetate
Non Proprietary Name: Megestrol Acetate
Active Ingredient(s): 800    mg/20mL & nbsp;   Megestrol Acetate
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Megestrol Acetate

Product NDC: 68094-518
Labeler Name: Precision Dose Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075671
Marketing Category: ANDA
Start Marketing Date: 20070109

Package Information of Megestrol Acetate

Package NDC: 68094-518-61
Package Description: 10 TRAY in 1 CASE (68094-518-61) > 10 CUP, UNIT-DOSE in 1 TRAY > 20 mL in 1 CUP, UNIT-DOSE (68094-518-59)

NDC Information of Megestrol Acetate

NDC Code 68094-518-61
Proprietary Name Megestrol Acetate
Package Description 10 TRAY in 1 CASE (68094-518-61) > 10 CUP, UNIT-DOSE in 1 TRAY > 20 mL in 1 CUP, UNIT-DOSE (68094-518-59)
Product NDC 68094-518
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Megestrol Acetate
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20070109
Marketing Category Name ANDA
Labeler Name Precision Dose Inc.
Substance Name MEGESTROL ACETATE
Strength Number 800
Strength Unit mg/20mL
Pharmaceutical Classes Progesterone Congeners [Chemical/Ingredient],Progestin [EPC]

Complete Information of Megestrol Acetate


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