megestrol acetate

Generic: megestrol acetate

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name megestrol acetate
Generic Name megestrol acetate
Labeler major pharmaceuticals
Dosage Form TABLET
Routes
ORAL
Active Ingredients

megestrol acetate 40 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-7236
Product ID 0904-7236_daa433c7-de6b-4e37-bdd9-2687d1a825ec
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA072423
Listing Expiration 2026-12-31
Marketing Start 2022-04-04

Pharmacologic Class

Classes
progesterone congeners [cs] progestin [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09047236
Hyphenated Format 0904-7236

Supplemental Identifiers

RxCUI
860221
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 ANDA072423 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (0904-7236-61) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

megestrol acetate (40 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "daa433c7-de6b-4e37-bdd9-2687d1a825ec", "openfda": {"unii": ["TJ2M0FR8ES"], "rxcui": ["860221"], "spl_set_id": ["2c755c6b-32e9-4029-8b70-855007f7375b"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7236-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7236-61", "marketing_start_date": "20220601"}], "brand_name": "Megestrol Acetate", "product_id": "0904-7236_daa433c7-de6b-4e37-bdd9-2687d1a825ec", "dosage_form": "TABLET", "pharm_class": ["Progesterone Congeners [CS]", "Progestin [EPC]"], "product_ndc": "0904-7236", "generic_name": "Megestrol Acetate", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Megestrol Acetate", "active_ingredients": [{"name": "MEGESTROL ACETATE", "strength": "40 mg/1"}], "application_number": "ANDA072423", "marketing_category": "ANDA", "marketing_start_date": "20220404", "listing_expiration_date": "20261231"}