megestrol acetate

Generic: megestrol acetate

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name megestrol acetate
Generic Name megestrol acetate
Labeler preferred pharmaceuticals inc.
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

megestrol acetate 40 mg/mL

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8714
Product ID 68788-8714_06743d22-d4e5-4543-9b01-e33febeba791
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075671
Listing Expiration 2026-12-31
Marketing Start 2024-07-12

Pharmacologic Class

Classes
progesterone congeners [cs] progestin [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687888714
Hyphenated Format 68788-8714

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
  • 240 mL in 1 BOTTLE, PLASTIC (68788-8714-2)
source: ndc

Packages (1)

Ingredients (1)

megestrol acetate (40 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "06743d22-d4e5-4543-9b01-e33febeba791", "openfda": {"unii": ["TJ2M0FR8ES"], "rxcui": ["860225"], "spl_set_id": ["edef65d1-d583-4cee-bb9a-515be84ac51d"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "240 mL in 1 BOTTLE, PLASTIC (68788-8714-2)", "package_ndc": "68788-8714-2", "marketing_start_date": "20240712"}], "brand_name": "Megestrol Acetate", "product_id": "68788-8714_06743d22-d4e5-4543-9b01-e33febeba791", "dosage_form": "SUSPENSION", "pharm_class": ["Progesterone Congeners [CS]", "Progestin [EPC]"], "product_ndc": "68788-8714", "generic_name": "Megestrol Acetate", "labeler_name": "Preferred Pharmaceuticals Inc.", "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": "20240712", "listing_expiration_date": "20261231"}