Package 17856-5310-1

{"route": ["ORAL"], "spl_id": "3ce758e5-06a4-7902-e063-6394a90a3bd4", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197803"], "spl_set_id": ["3ce7549f-e4db-9f89-e063-6294a90a126d"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "50 CUP, UNIT-DOSE in 1 CASE (17856-5310-1)  / 30 mL in 1 CUP, UNIT-DOSE", "package_ndc": "17856-5310-1", "marketing_start_date": "20250821"}], "brand_name": "Ibuprofen", "product_id": "17856-5310_3ce758e5-06a4-7902-e063-6394a90a3bd4", "dosage_form": "SUSPENSION", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "17856-5310", "generic_name": "Ibuprofen", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "100 mg/5mL"}], "application_number": "ANDA074937", "marketing_category": "ANDA", "marketing_start_date": "19990207", "listing_expiration_date": "20261231"}