Package 50090-6629-0

Brand: hydroxychloroquine sulfate

Generic: hydroxychloroquine sulfate
NDC Package

Package Facts

Identity

Package NDC 50090-6629-0
Digits Only 5009066290
Product NDC 50090-6629
Product ID 50090-6629_987a57ba-5ae5-48e9-ab97-4c293c2cabc0
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-6629-0)

Marketing

Marketing Status
Marketed Since 2023-08-25
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": "987a57ba-5ae5-48e9-ab97-4c293c2cabc0", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["1a1fb21d-a01c-4d50-8764-cdd6c20d9569"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6629-0)", "package_ndc": "50090-6629-0", "marketing_start_date": "20230825"}], "brand_name": "Hydroxychloroquine sulfate", "product_id": "50090-6629_987a57ba-5ae5-48e9-ab97-4c293c2cabc0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "50090-6629", "generic_name": "Hydroxychloroquine sulfate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxychloroquine sulfate", "active_ingredients": [{"name": "HYDROXYCHLOROQUINE SULFATE", "strength": "200 mg/1"}], "application_number": "ANDA040657", "marketing_category": "ANDA", "marketing_start_date": "20191001", "listing_expiration_date": "20261231"}