Package 60760-865-12

Brand: butalbital, acetaminophen and caffeine

Generic: butalbital, acetaminophen and caffeine
NDC Package

Package Facts

Identity

Package NDC 60760-865-12
Digits Only 6076086512
Product NDC 60760-865
Description

12 TABLET in 1 BOTTLE, PLASTIC (60760-865-12)

Marketing

Marketing Status
Marketed Since 2025-05-19
Brand butalbital, acetaminophen and caffeine
Generic butalbital, acetaminophen and caffeine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "36229f4e-5921-2fcd-e063-6294a90af60d", "openfda": {"nui": ["N0000175693", "M0002177", "N0000175739", "N0000175729", "N0000175790", "M0023046"], "unii": ["362O9ITL9D", "KHS0AZ4JVK", "3G6A5W338E"], "rxcui": ["238154"], "spl_set_id": ["36229f70-aa73-b112-e063-6394a90a5b49"], "pharm_class_cs": ["Barbiturates [CS]", "Xanthines [CS]"], "pharm_class_pe": ["Central Nervous System Stimulation [PE]"], "pharm_class_epc": ["Barbiturate [EPC]", "Central Nervous System Stimulant [EPC]", "Methylxanthine [EPC]"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET in 1 BOTTLE, PLASTIC (60760-865-12)", "package_ndc": "60760-865-12", "marketing_start_date": "20250519"}], "brand_name": "Butalbital, Acetaminophen and Caffeine", "product_id": "60760-865_36229f4e-5921-2fcd-e063-6294a90af60d", "dosage_form": "TABLET", "pharm_class": ["Barbiturate [EPC]", "Barbiturates [CS]", "Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]", "Methylxanthine [EPC]", "Xanthines [CS]"], "product_ndc": "60760-865", "dea_schedule": "CIII", "generic_name": "Butalbital, Acetaminophen and Caffeine", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Butalbital, Acetaminophen and Caffeine", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "BUTALBITAL", "strength": "50 mg/1"}, {"name": "CAFFEINE", "strength": "40 mg/1"}], "application_number": "ANDA040864", "marketing_category": "ANDA", "marketing_start_date": "20220629", "listing_expiration_date": "20261231"}