Package 50268-412-15

Brand: hydroxychloroquine sulfate

Generic: hydroxychloroquine sulfate
NDC Package

Package Facts

Identity

Package NDC 50268-412-15
Digits Only 5026841215
Product NDC 50268-412
Product ID 50268-412_47e560c6-bd1f-1264-e063-6394a90a0048
Description

50 BLISTER PACK in 1 BOX (50268-412-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-412-11)

Marketing

Marketing Status
Marketed Since 2020-05-15
Brand hydroxychloroquine sulfate
Generic hydroxychloroquine sulfate
Sample Package No

Linked Drug Pages (1)

HYDROXYCHLOROQUINE SULFATE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47e560c6-bd1f-1264-e063-6394a90a0048", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["a5b3455a-e842-7d4b-e053-2995a90adee3"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-412-15)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-412-11)", "package_ndc": "50268-412-15", "marketing_start_date": "20200515"}], "brand_name": "HYDROXYCHLOROQUINE SULFATE", "product_id": "50268-412_47e560c6-bd1f-1264-e063-6394a90a0048", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "50268-412", "generic_name": "HYDROXYCHLOROQUINE SULFATE", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROXYCHLOROQUINE SULFATE", "active_ingredients": [{"name": "HYDROXYCHLOROQUINE SULFATE", "strength": "200 mg/1"}], "application_number": "ANDA210441", "marketing_category": "ANDA", "marketing_start_date": "20200515", "listing_expiration_date": "20271231"}