Package 72090-034-02
Brand: aspirin pain reliver
Generic: aspirinPackage Facts
Identity
Package NDC
72090-034-02
Digits Only
7209003402
Product NDC
72090-034
Description
1000 TABLET in 1 BOTTLE (72090-034-02)
Marketing
Marketing Status
Brand
aspirin pain reliver
Generic
aspirin
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ee1c0ed7-e39d-4d8b-b7b8-fb10ce496321", "openfda": {"nui": ["N0000000160", "N0000008836", "M0001335", "N0000175722", "N0000175578", "N0000008832"], "upc": ["0372090002937"], "unii": ["R16CO5Y76E"], "rxcui": ["308416"], "spl_set_id": ["8dc29957-2ac1-47f8-89fd-a6bcf97ee3d3"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_pe": ["Decreased Prostaglandin Production [PE]", "Decreased Platelet Aggregation [PE]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]", "Platelet Aggregation Inhibitor [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Pioneer Life Sciences, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (72090-034-01)", "package_ndc": "72090-034-01", "marketing_start_date": "20240912"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (72090-034-02)", "package_ndc": "72090-034-02", "marketing_start_date": "20240912"}], "brand_name": "Aspirin Pain reliver", "product_id": "72090-034_ee1c0ed7-e39d-4d8b-b7b8-fb10ce496321", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Platelet Aggregation [PE]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]", "Platelet Aggregation Inhibitor [EPC]"], "product_ndc": "72090-034", "generic_name": "Aspirin", "labeler_name": "Pioneer Life Sciences, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Aspirin Pain reliver", "active_ingredients": [{"name": "ASPIRIN", "strength": "81 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240912", "listing_expiration_date": "20261231"}