Esgic - 0535-0011-01 - (butalbital, acetaminophen and caffeine)

Alphabetical Index


Drug Information of Esgic

Product NDC: 0535-0011
Proprietary Name: Esgic
Non Proprietary Name: butalbital, acetaminophen and caffeine
Active Ingredient(s): 325; 50; 40    mg/1; mg/1; mg/1 & nbsp;   butalbital, acetaminophen and caffeine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Esgic

Product NDC: 0535-0011
Labeler Name: Forest Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089175
Marketing Category: ANDA
Start Marketing Date: 19970601

Package Information of Esgic

Package NDC: 0535-0011-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (0535-0011-01)

NDC Information of Esgic

NDC Code 0535-0011-01
Proprietary Name Esgic
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (0535-0011-01)
Product NDC 0535-0011
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name butalbital, acetaminophen and caffeine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19970601
Marketing Category Name ANDA
Labeler Name Forest Laboratories, Inc.
Substance Name ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Strength Number 325; 50; 40
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes Barbiturate [EPC],Barbiturates [Chemical/Ingredient],Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE],Methylxanthine [EPC],Xanthines [Chemical/Ingredient]

Complete Information of Esgic


General Information