Package 68180-560-06

Brand: quinine sulfate

Generic: quinine sulfate
NDC Package

Package Facts

Identity

Package NDC 68180-560-06
Digits Only 6818056006
Product NDC 68180-560
Product ID 68180-560_8cd4d427-50ac-4f9c-a029-e7c2d063679a
Description

30 CAPSULE in 1 BOTTLE (68180-560-06)

Marketing

Marketing Status
Marketed Since 2015-08-04
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": "8cd4d427-50ac-4f9c-a029-e7c2d063679a", "openfda": {"unii": ["KF7Z0E0Q2B"], "rxcui": ["997010"], "spl_set_id": ["1f32f05c-a215-40be-b951-e41a7b54a8a0"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68180-560-06)", "package_ndc": "68180-560-06", "marketing_start_date": "20150804"}], "brand_name": "QUININE SULFATE", "product_id": "68180-560_8cd4d427-50ac-4f9c-a029-e7c2d063679a", "dosage_form": "CAPSULE", "pharm_class": ["Antimalarial [EPC]"], "product_ndc": "68180-560", "generic_name": "QUININE SULFATE", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "QUININE SULFATE", "active_ingredients": [{"name": "QUININE SULFATE", "strength": "324 mg/1"}], "application_number": "ANDA203112", "marketing_category": "ANDA", "marketing_start_date": "20150804", "listing_expiration_date": "20261231"}