Package 43063-721-28

Brand: primaquine phosphate

Generic: primaquine phosphate
NDC Package

Package Facts

Identity

Package NDC 43063-721-28
Digits Only 4306372128
Product NDC 43063-721
Description

28 TABLET in 1 BOTTLE, PLASTIC (43063-721-28)

Marketing

Marketing Status
Marketed Since 2016-10-17
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": "36c0e266-7161-2887-e063-6294a90a9fc1", "openfda": {"upc": ["0343063721285"], "unii": ["H0982HF78B"], "rxcui": ["904170"], "spl_set_id": ["3f16166d-678e-51aa-e054-00144ff88e88"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET in 1 BOTTLE, PLASTIC (43063-721-14)", "package_ndc": "43063-721-14", "marketing_start_date": "20161017"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE, PLASTIC (43063-721-28)", "package_ndc": "43063-721-28", "marketing_start_date": "20161017"}], "brand_name": "Primaquine Phosphate", "product_id": "43063-721_36c0e266-7161-2887-e063-6294a90a9fc1", "dosage_form": "TABLET", "pharm_class": ["Antimalarial [EPC]"], "product_ndc": "43063-721", "generic_name": "Primaquine Phosphate", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Primaquine Phosphate", "active_ingredients": [{"name": "PRIMAQUINE PHOSPHATE", "strength": "15 mg/1"}], "application_number": "ANDA204476", "marketing_category": "ANDA", "marketing_start_date": "20140801", "listing_expiration_date": "20261231"}