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Megestrol Acetate - 68094-528-62 - (Megestrol Acetate)

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Drug Information of Megestrol Acetate

Product NDC: 68094-528
Proprietary Name: Megestrol Acetate
Non Proprietary Name: Megestrol Acetate
Active Ingredient(s): 400    mg/10mL & nbsp;   Megestrol Acetate
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Megestrol Acetate

Product NDC: 68094-528
Labeler Name: Precision Dose Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075671
Marketing Category: ANDA
Start Marketing Date: 20040225

Package Information of Megestrol Acetate

Package NDC: 68094-528-62
Package Description: 3 TRAY in 1 CASE (68094-528-62) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (68094-528-59)

NDC Information of Megestrol Acetate

NDC Code 68094-528-62
Proprietary Name Megestrol Acetate
Package Description 3 TRAY in 1 CASE (68094-528-62) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (68094-528-59)
Product NDC 68094-528
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Megestrol Acetate
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20040225
Marketing Category Name ANDA
Labeler Name Precision Dose Inc.
Substance Name MEGESTROL ACETATE
Strength Number 400
Strength Unit mg/10mL
Pharmaceutical Classes Progesterone Congeners [Chemical/Ingredient],Progestin [EPC]

Complete Information of Megestrol Acetate


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