Package 50742-238-30

Brand: quinine sulfate

Generic: quinine sulfate
NDC Package

Package Facts

Identity

Package NDC 50742-238-30
Digits Only 5074223830
Product NDC 50742-238
Product ID 50742-238_0a0b38d3-828f-4828-8d8c-92933872aa4f
Description

30 CAPSULE in 1 BOTTLE, PLASTIC (50742-238-30)

Marketing

Marketing Status
Marketed Since 2017-12-11
Brand quinine sulfate
Generic quinine sulfate
Sample Package No

Linked Drug Pages (1)

QUININE SULFATE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0a0b38d3-828f-4828-8d8c-92933872aa4f", "openfda": {"upc": ["0350742238309"], "unii": ["KF7Z0E0Q2B"], "rxcui": ["997010"], "spl_set_id": ["b2f73c64-b92c-49bf-ad39-e32ac83e4d3d"], "manufacturer_name": ["Ingenus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (50742-238-30)", "package_ndc": "50742-238-30", "marketing_start_date": "20171211"}], "brand_name": "QUININE SULFATE", "product_id": "50742-238_0a0b38d3-828f-4828-8d8c-92933872aa4f", "dosage_form": "CAPSULE", "pharm_class": ["Antimalarial [EPC]"], "product_ndc": "50742-238", "generic_name": "QUININE SULFATE", "labeler_name": "Ingenus Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "QUININE SULFATE", "active_ingredients": [{"name": "QUININE SULFATE", "strength": "324 mg/1"}], "application_number": "ANDA204372", "marketing_category": "ANDA", "marketing_start_date": "20171211", "listing_expiration_date": "20261231"}