Margesic - 0682-0804-01 - (butalbital, acetaminophen and caffeine)

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Drug Information of Margesic

Product NDC: 0682-0804
Proprietary Name: Margesic
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): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Margesic

Product NDC: 0682-0804
Labeler Name: Marnel Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089007
Marketing Category: ANDA
Start Marketing Date: 19940601

Package Information of Margesic

Package NDC: 0682-0804-01
Package Description: 100 CAPSULE in 1 BOTTLE, PLASTIC (0682-0804-01)

NDC Information of Margesic

NDC Code 0682-0804-01
Proprietary Name Margesic
Package Description 100 CAPSULE in 1 BOTTLE, PLASTIC (0682-0804-01)
Product NDC 0682-0804
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name butalbital, acetaminophen and caffeine
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19940601
Marketing Category Name ANDA
Labeler Name Marnel Pharmaceuticals, 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 Margesic


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