Alagesic - 50991-514-01 - (butalbital, acetaminophen and caffeine)

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Drug Information of Alagesic

Product NDC: 50991-514
Proprietary Name: Alagesic
Non Proprietary Name: butalbital, acetaminophen and caffeine
Active Ingredient(s): 325; 50; 40    mg/15mL; mg/15mL; mg/15mL & nbsp;   butalbital, acetaminophen and caffeine
Administration Route(s): ORAL
Dosage Form(s): SYRUP
Coding System: National Drug Codes(NDC)

Labeler Information of Alagesic

Product NDC: 50991-514
Labeler Name: Poly Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089175
Marketing Category: ANDA
Start Marketing Date: 20100215

Package Information of Alagesic

Package NDC: 50991-514-01
Package Description: 30 mL in 1 BOTTLE (50991-514-01)

NDC Information of Alagesic

NDC Code 50991-514-01
Proprietary Name Alagesic
Package Description 30 mL in 1 BOTTLE (50991-514-01)
Product NDC 50991-514
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name butalbital, acetaminophen and caffeine
Dosage Form Name SYRUP
Route Name ORAL
Start Marketing Date 20100215
Marketing Category Name ANDA
Labeler Name Poly Pharmaceuticals, Inc.
Substance Name ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Strength Number 325; 50; 40
Strength Unit mg/15mL; mg/15mL; mg/15mL
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 Alagesic


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