megestrol acetate
Generic: megestrol acetate
Labeler: major pharmaceuticalsDrug Facts
Product Profile
Brand Name
megestrol acetate
Generic Name
megestrol acetate
Labeler
major pharmaceuticals
Dosage Form
SUSPENSION
Routes
Active Ingredients
megestrol acetate 400 mg/10mL
Manufacturer
Identifiers & Regulatory
Product NDC
0904-7577
Product ID
0904-7577_1843fe79-7628-4f8e-9b51-e0be7562e43d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077404
Listing Expiration
2027-12-31
Marketing Start
2025-12-29
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
09047577
Hyphenated Format
0904-7577
Supplemental Identifiers
RxCUI
UPC
UNII
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
ANDA077404 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 400 mg/10mL
Packaging
- 4 TRAY in 1 CASE (0904-7577-18) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0904-7577-66)
- 10 TRAY in 1 CASE (0904-7577-72) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0904-7577-66)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1843fe79-7628-4f8e-9b51-e0be7562e43d", "openfda": {"upc": ["0309047577668"], "unii": ["TJ2M0FR8ES"], "rxcui": ["860225"], "spl_set_id": ["e44cf173-991b-43cf-93f2-e0efaa4cc29a"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "4 TRAY in 1 CASE (0904-7577-18) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0904-7577-66)", "package_ndc": "0904-7577-18", "marketing_start_date": "20260115"}, {"sample": false, "description": "10 TRAY in 1 CASE (0904-7577-72) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0904-7577-66)", "package_ndc": "0904-7577-72", "marketing_start_date": "20251229"}], "brand_name": "Megestrol Acetate", "product_id": "0904-7577_1843fe79-7628-4f8e-9b51-e0be7562e43d", "dosage_form": "SUSPENSION", "pharm_class": ["Progesterone Congeners [CS]", "Progestin [EPC]"], "product_ndc": "0904-7577", "generic_name": "Megestrol Acetate", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Megestrol Acetate", "active_ingredients": [{"name": "MEGESTROL ACETATE", "strength": "400 mg/10mL"}], "application_number": "ANDA077404", "marketing_category": "ANDA", "marketing_start_date": "20251229", "listing_expiration_date": "20271231"}