Home NDC 80425-0570 Butalbital, Acetaminophen, Caffeine
Product NDC 80425-0570
11-digit product format 804250570
Labeler code 80425
Product ID 80425-0570_4871bd26-4d42-a212-e063-6294a90a13ca
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Butalbital, Acetaminophen, and Caffeine
Dosage form TABLET
Route ORAL
Labeler Advanced Rx of Tennessee, LLC
Application ANDA209587
Marketing category ANDA
Marketing start 2026-01-08
Substance ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Active strength 325; 50; 40 mg/1; mg/1; mg/1
Pharmacologic classes Barbiturate [EPC], Barbiturates [CS], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Methylxanthine [EPC], Xanthines [CS]
DEA schedule CIII
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Butalbital, Acetaminophen, Caffeine
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 325 mg/1 BUTALBITAL 50 mg/1 CAFFEINE 40 mg/1
Harmonized Identifiers# Field, Values table Field Values Unii 362O9ITL9D, KHS0AZ4JVK, 3G6A5W338E Rxcui 238154
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 80425-0570-1 Butalbital, Acetaminophen, Caffeine 30 in 1 BOTTLE TABLET 30 1 80425-0570-2 Butalbital, Acetaminophen, Caffeine 60 in 1 BOTTLE TABLET 60 1 80425-0570-3 Butalbital, Acetaminophen, Caffeine 90 in 1 BOTTLE TABLET 90 1
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 80425-0570-1 80425057001 30 TABLET in 1 BOTTLE (80425-0570-1) 30 tablet 2026-01-08 No No Historical 80425-0570-2 80425057002 60 TABLET in 1 BOTTLE (80425-0570-2) 60 tablet 2026-01-08 No No Historical 80425-0570-3 80425057003 90 TABLET in 1 BOTTLE (80425-0570-3) 90 tablet 2026-01-08 No No Historical