megestrol acetate

Generic: megestrol acetate

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name megestrol acetate
Generic Name megestrol acetate
Labeler teva pharmaceuticals usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

megestrol acetate 20 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0555-0606
Product ID 0555-0606_6f22887e-a442-4505-bd99-00042e4075c7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074621
Listing Expiration 2026-12-31
Marketing Start 1996-10-25

Pharmacologic Class

Classes
progesterone congeners [cs] progestin [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05550606
Hyphenated Format 0555-0606

Supplemental Identifiers

RxCUI
860215 860221
UPC
0305550607021 0305550606024
UNII
TJ2M0FR8ES

Packaging Origin

Original Packager
true

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 ANDA074621 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (0555-0606-02)
source: ndc

Packages (1)

Ingredients (1)

megestrol acetate (20 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6f22887e-a442-4505-bd99-00042e4075c7", "openfda": {"upc": ["0305550607021", "0305550606024"], "unii": ["TJ2M0FR8ES"], "rxcui": ["860215", "860221"], "spl_set_id": ["66573d39-f2a7-49fd-9ed2-97ac8f6e8456"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0555-0606-02)", "package_ndc": "0555-0606-02", "marketing_start_date": "19961025"}], "brand_name": "Megestrol Acetate", "product_id": "0555-0606_6f22887e-a442-4505-bd99-00042e4075c7", "dosage_form": "TABLET", "pharm_class": ["Progesterone Congeners [CS]", "Progestin [EPC]"], "product_ndc": "0555-0606", "generic_name": "Megestrol Acetate", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Megestrol Acetate", "active_ingredients": [{"name": "MEGESTROL ACETATE", "strength": "20 mg/1"}], "application_number": "ANDA074621", "marketing_category": "ANDA", "marketing_start_date": "19961025", "listing_expiration_date": "20261231"}