Package 68788-7747-3

Brand: hydroxychloroquine sulfate

Generic: hydroxychloroquine sulfate
NDC Package

Package Facts

Identity

Package NDC 68788-7747-3
Digits Only 6878877473
Product NDC 68788-7747
Product ID 68788-7747_8f6c96df-61ea-4abe-8d96-5dc5caa82ace
Description

30 TABLET, FILM COATED in 1 BOTTLE (68788-7747-3)

Marketing

Marketing Status
Marketed Since 2020-07-01
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": "8f6c96df-61ea-4abe-8d96-5dc5caa82ace", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["d6c8ee2e-116e-4167-8d1a-bd570a1ce672"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68788-7747-2)", "package_ndc": "68788-7747-2", "marketing_start_date": "20200701"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-7747-3)", "package_ndc": "68788-7747-3", "marketing_start_date": "20200701"}], "brand_name": "Hydroxychloroquine sulfate", "product_id": "68788-7747_8f6c96df-61ea-4abe-8d96-5dc5caa82ace", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "68788-7747", "generic_name": "Hydroxychloroquine sulfate", "labeler_name": "Preferred Pharmaceuticals, Inc.", "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": "20200701", "listing_expiration_date": "20261231"}