Package 43063-934-01

Brand: allopurinol

Generic: allopurinol
NDC Package

Package Facts

Identity

Package NDC 43063-934-01
Digits Only 4306393401
Product NDC 43063-934
Description

100 TABLET in 1 BOTTLE, PLASTIC (43063-934-01)

Marketing

Marketing Status
Marketed Since 2019-01-29
Brand allopurinol
Generic allopurinol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c4ea0d1-3007-7432-e063-6394a90a58ff", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197320"], "spl_set_id": ["f1c11f74-1de2-484c-b40b-d0013e8fd01a"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (43063-934-01)", "package_ndc": "43063-934-01", "marketing_start_date": "20190129"}], "brand_name": "Allopurinol", "product_id": "43063-934_2c4ea0d1-3007-7432-e063-6394a90a58ff", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "43063-934", "generic_name": "Allopurinol", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "300 mg/1"}], "application_number": "ANDA071450", "marketing_category": "ANDA", "marketing_start_date": "19870109", "listing_expiration_date": "20261231"}