NDC 63629-7631

Megestrol Acetate

Megestrol Acetate

Megestrol Acetate is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Megestrol Acetate.

Product ID63629-7631_656cd5ef-0776-478a-9b60-b81c1554eccc
NDC63629-7631
Product TypeHuman Prescription Drug
Proprietary NameMegestrol Acetate
Generic NameMegestrol Acetate
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1988-08-08
Marketing CategoryANDA / ANDA
Application NumberANDA072423
Labeler NameBryant Ranch Prepack
Substance NameMEGESTROL ACETATE
Active Ingredient Strength40 mg/1
Pharm ClassesProgesterone Congeners [CS],Progestin [EPC]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 63629-7631-1

30 TABLET in 1 BOTTLE (63629-7631-1)
Marketing Start Date2018-05-18
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63629-7631-2 [63629763102]

Megestrol Acetate TABLET
Marketing CategoryANDA
Application NumberANDA072423
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-05-18
Inactivation Date2020-01-31

NDC 63629-7631-1 [63629763101]

Megestrol Acetate TABLET
Marketing CategoryANDA
Application NumberANDA072423
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-05-18
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
MEGESTROL ACETATE40 mg/1

OpenFDA Data

SPL SET ID:8b035f11-35be-4f7c-9daf-e2bc164a6bb4
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 860221
  • Pharmacological Class

    • Progesterone Congeners [CS]
    • Progestin [EPC]