Package 50102-220-23

Brand: aubra eq

Generic: levonorgestrel and ethinyl estradiol
NDC Package

Package Facts

Identity

Package NDC 50102-220-23
Digits Only 5010222023
Product NDC 50102-220
Product ID 50102-220_168ba8ff-87c7-4c10-a48d-6fe29555a997
Description

3 POUCH in 1 CARTON (50102-220-23) / 1 BLISTER PACK in 1 POUCH (50102-220-21) / 1 KIT in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2016-11-14
Brand aubra eq
Generic levonorgestrel and ethinyl estradiol
Sample Package No

Linked Drug Pages (1)

Aubra EQ ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "168ba8ff-87c7-4c10-a48d-6fe29555a997", "openfda": {"rxcui": ["242297", "748797", "748868", "1440185"], "spl_set_id": ["61207a91-8b3c-4231-b98f-3cb9f4a4be09"], "manufacturer_name": ["Afaxys Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 POUCH in 1 CARTON (50102-220-23)  / 1 BLISTER PACK in 1 POUCH (50102-220-21)  / 1 KIT in 1 BLISTER PACK", "package_ndc": "50102-220-23", "marketing_start_date": "20161114"}], "brand_name": "Aubra EQ", "product_id": "50102-220_168ba8ff-87c7-4c10-a48d-6fe29555a997", "dosage_form": "KIT", "product_ndc": "50102-220", "generic_name": "Levonorgestrel and Ethinyl Estradiol", "labeler_name": "Afaxys Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aubra EQ", "application_number": "ANDA206886", "marketing_category": "ANDA", "marketing_start_date": "20161114", "listing_expiration_date": "20261231"}