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Pain Reliever Plus - 0904-5135-59 - (Acetaminophen, Aspirin and caffeine)

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Drug Information of Pain Reliever Plus

Product NDC: 0904-5135
Proprietary Name: Pain Reliever Plus
Non Proprietary Name: Acetaminophen, Aspirin and caffeine
Active Ingredient(s): 250; 250; 65    mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Aspirin and caffeine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Pain Reliever Plus

Product NDC: 0904-5135
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 19921117

Package Information of Pain Reliever Plus

Package NDC: 0904-5135-59
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (0904-5135-59) > 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

NDC Information of Pain Reliever Plus

NDC Code 0904-5135-59
Proprietary Name Pain Reliever Plus
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (0904-5135-59) > 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product NDC 0904-5135
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Aspirin and caffeine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19921117
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Major Pharmaceuticals
Substance Name ACETAMINOPHEN; ASPIRIN; CAFFEINE
Strength Number 250; 250; 65
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of Pain Reliever Plus


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