Package 0555-0606-02

Brand: megestrol acetate

Generic: megestrol acetate
NDC Package

Package Facts

Identity

Package NDC 0555-0606-02
Digits Only 0555060602
Product NDC 0555-0606
Product ID 0555-0606_6f22887e-a442-4505-bd99-00042e4075c7
Description

100 TABLET in 1 BOTTLE (0555-0606-02)

Marketing

Marketing Status
Marketed Since 1996-10-25
Brand megestrol acetate
Generic megestrol acetate
Sample Package No

Linked Drug Pages (1)

Megestrol Acetate ndc-match (0.95)

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"}