Package 68071-2332-1

Brand: hydroxychloroquine sulfate

Generic: hydroxychloroquine sulfate
NDC Package

Package Facts

Identity

Package NDC 68071-2332-1
Digits Only 6807123321
Product NDC 68071-2332
Product ID 68071-2332_3c6be558-7aab-97e6-e063-6294a90af84f
Description

100 TABLET, FILM COATED in 1 BOTTLE (68071-2332-1)

Marketing

Marketing Status
Marketed Since 2021-01-14
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": "3c6be558-7aab-97e6-e063-6294a90af84f", "openfda": {"upc": ["0368071233216"], "unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["b8e3a352-a1e3-e672-e053-2a95a90a641c"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68071-2332-1)", "package_ndc": "68071-2332-1", "marketing_start_date": "20210114"}], "brand_name": "Hydroxychloroquine sulfate", "product_id": "68071-2332_3c6be558-7aab-97e6-e063-6294a90af84f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "68071-2332", "generic_name": "Hydroxychloroquine sulfate", "labeler_name": "NuCare 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": "20191001", "listing_expiration_date": "20261231"}