Package 0024-1596-01

Brand: primaquine phosphate

Generic: primaquine phosphate
NDC Package

Package Facts

Identity

Package NDC 0024-1596-01
Digits Only 0024159601
Product NDC 0024-1596
Description

100 TABLET, FILM COATED in 1 BOTTLE (0024-1596-01)

Marketing

Marketing Status
Marketed Since 2011-04-15
Brand primaquine phosphate
Generic primaquine phosphate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7e15f87d-f34f-4ec2-9da8-a041db792623", "openfda": {"unii": ["H0982HF78B"], "rxcui": ["904170"], "spl_set_id": ["1bfbf4ae-81b8-4160-a00d-6322aadd4b59"], "manufacturer_name": ["Sanofi-Aventis U.S. LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0024-1596-01)", "package_ndc": "0024-1596-01", "marketing_start_date": "20110415"}], "brand_name": "Primaquine Phosphate", "product_id": "0024-1596_7e15f87d-f34f-4ec2-9da8-a041db792623", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]"], "product_ndc": "0024-1596", "generic_name": "Primaquine Phosphate", "labeler_name": "Sanofi-Aventis U.S. LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Primaquine Phosphate", "active_ingredients": [{"name": "PRIMAQUINE PHOSPHATE", "strength": "15 mg/1"}], "application_number": "NDA008316", "marketing_category": "NDA", "marketing_start_date": "20110415", "listing_expiration_date": "20271231"}