megestrol acetate

Generic: megestrol acetate

Labeler: kesin pharma corporation
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name megestrol acetate
Generic Name megestrol acetate
Labeler kesin pharma corporation
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

megestrol acetate 40 mg/mL

Manufacturer
Kesin Pharma Corporation

Identifiers & Regulatory

Product NDC 81033-150
Product ID 81033-150_3dd3d565-dc60-0c31-e063-6394a90a46e3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075671
Listing Expiration 2026-12-31
Marketing Start 2025-08-07

Pharmacologic Class

Classes
progesterone congeners [cs] progestin [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 81033150
Hyphenated Format 81033-150

Supplemental Identifiers

RxCUI
860225
UNII
TJ2M0FR8ES

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name megestrol acetate (source: ndc)
Generic Name megestrol acetate (source: ndc)
Application Number ANDA075671 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/mL
source: ndc
Packaging
  • 30 CUP, UNIT-DOSE in 1 CARTON (81033-150-43) / 20 mL in 1 CUP, UNIT-DOSE (81033-150-20)
  • 40 CUP, UNIT-DOSE in 1 CARTON (81033-150-44) / 10 mL in 1 CUP, UNIT-DOSE (81033-150-10)
  • 100 CUP, UNIT-DOSE in 1 CASE (81033-150-52) / 10 mL in 1 CUP, UNIT-DOSE (81033-150-10)
source: ndc

Packages (3)

81033-150-43 30 CUP, UNIT-DOSE in 1 CARTON (81033-150-43) / 20 mL in 1 CUP, UNIT-DOSE (81033-150-20) 81033-150-44 40 CUP, UNIT-DOSE in 1 CARTON (81033-150-44) / 10 mL in 1 CUP, UNIT-DOSE (81033-150-10) 81033-150-52 100 CUP, UNIT-DOSE in 1 CASE (81033-150-52) / 10 mL in 1 CUP, UNIT-DOSE (81033-150-10)

Ingredients (1)

megestrol acetate (40 mg/mL)

Linked Drug Pages (1)

Megestrol Acetate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3dd3d565-dc60-0c31-e063-6394a90a46e3", "openfda": {"unii": ["TJ2M0FR8ES"], "rxcui": ["860225"], "spl_set_id": ["3bc8708e-a52d-fda2-e063-6294a90a0fbc"], "manufacturer_name": ["Kesin Pharma Corporation"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CUP, UNIT-DOSE in 1 CARTON (81033-150-43)  / 20 mL in 1 CUP, UNIT-DOSE (81033-150-20)", "package_ndc": "81033-150-43", "marketing_start_date": "20250807"}, {"sample": false, "description": "40 CUP, UNIT-DOSE in 1 CARTON (81033-150-44)  / 10 mL in 1 CUP, UNIT-DOSE (81033-150-10)", "package_ndc": "81033-150-44", "marketing_start_date": "20250807"}, {"sample": false, "description": "100 CUP, UNIT-DOSE in 1 CASE (81033-150-52)  / 10 mL in 1 CUP, UNIT-DOSE (81033-150-10)", "package_ndc": "81033-150-52", "marketing_start_date": "20250807"}], "brand_name": "Megestrol Acetate", "product_id": "81033-150_3dd3d565-dc60-0c31-e063-6394a90a46e3", "dosage_form": "SUSPENSION", "pharm_class": ["Progesterone Congeners [CS]", "Progestin [EPC]"], "product_ndc": "81033-150", "generic_name": "Megestrol Acetate", "labeler_name": "Kesin Pharma Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Megestrol Acetate", "active_ingredients": [{"name": "MEGESTROL ACETATE", "strength": "40 mg/mL"}], "application_number": "ANDA075671", "marketing_category": "ANDA", "marketing_start_date": "20250807", "listing_expiration_date": "20261231"}