Package 60760-134-90

Brand: allopurinol

Generic: allopurinol
NDC Package

Package Facts

Identity

Package NDC 60760-134-90
Digits Only 6076013490
Product NDC 60760-134
Description

90 TABLET in 1 BOTTLE, PLASTIC (60760-134-90)

Marketing

Marketing Status
Marketed Since 2017-12-20
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": "f06e6e94-f0e4-7303-e053-2a95a90afa61", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319"], "spl_set_id": ["60cdd69c-fd25-77de-e053-2a91aa0ad472"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["St. Mary's Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (60760-134-90)", "package_ndc": "60760-134-90", "marketing_start_date": "20171220"}], "brand_name": "Allopurinol", "product_id": "60760-134_f06e6e94-f0e4-7303-e053-2a95a90afa61", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "60760-134", "generic_name": "allopurinol", "labeler_name": "St. Mary's Medical Park Pharmacy", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "100 mg/1"}], "application_number": "ANDA203154", "marketing_category": "ANDA", "marketing_start_date": "20171220", "listing_expiration_date": "20261231"}