Home NDC 73352-917 Cafergot
Product NDC 73352-917
11-digit product format 733520917
Labeler code 73352
Product ID 73352-917_4db7f801-0dea-0ec8-e063-6294a90a2636
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name ergotamine tartrate and caffeine
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Trifluent Pharma, LLC
Application ANDA040590
Marketing category ANDA
Marketing start 2026-03-23
Substance CAFFEINE; ERGOTAMINE TARTRATE
Active strength 100; 1 mg/1; mg/1
Pharmacologic classes Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Ergotamine Derivative [EPC], Ergotamines [CS], Methylxanthine [EPC], Xanthines [CS]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Cafergot
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CAFFEINE 100 mg/1 ERGOTAMINE TARTRATE 1 mg/1
Harmonized Identifiers# Field, Values table Field Values Unii 3G6A5W338E, MRU5XH3B48 Rxcui 1293504, 1293506
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 73352-917-40 Cafergot 40 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 40 1
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 73352-917-40 73352091740 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (73352-917-40) 2026-03-23 No No Current