Package 71205-448-12

Brand: plaquenil

Generic: hydroxychloroquine sulfate
NDC Package

Package Facts

Identity

Package NDC 71205-448-12
Digits Only 7120544812
Product NDC 71205-448
Description

12 TABLET in 1 BOTTLE (71205-448-12)

Marketing

Marketing Status
Marketed Since 2020-04-08
Brand plaquenil
Generic hydroxychloroquine sulfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8aec894d-5711-4079-b167-240713bf04f2", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["979092", "979094"], "spl_set_id": ["8aec894d-5711-4079-b167-240713bf04f2"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET in 1 BOTTLE (71205-448-12)", "package_ndc": "71205-448-12", "marketing_start_date": "20200408"}], "brand_name": "Plaquenil", "product_id": "71205-448_8aec894d-5711-4079-b167-240713bf04f2", "dosage_form": "TABLET", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "71205-448", "generic_name": "Hydroxychloroquine Sulfate", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Plaquenil", "active_ingredients": [{"name": "HYDROXYCHLOROQUINE SULFATE", "strength": "200 mg/1"}], "application_number": "NDA009768", "marketing_category": "NDA", "marketing_start_date": "20130628", "listing_expiration_date": "20261231"}