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Rapid Release Pain Reliever - 0363-0519-20 - (Acetaminophen)

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Drug Information of Rapid Release Pain Reliever

Product NDC: 0363-0519
Proprietary Name: Rapid Release Pain Reliever
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 500    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, GELATIN COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Rapid Release Pain Reliever

Product NDC: 0363-0519
Labeler Name: WALGREEN CO.
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20040510

Package Information of Rapid Release Pain Reliever

Package NDC: 0363-0519-20
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (0363-0519-20) > 225 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC

NDC Information of Rapid Release Pain Reliever

NDC Code 0363-0519-20
Proprietary Name Rapid Release Pain Reliever
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (0363-0519-20) > 225 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC
Product NDC 0363-0519
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name CAPSULE, GELATIN COATED
Route Name ORAL
Start Marketing Date 20040510
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name WALGREEN CO.
Substance Name ACETAMINOPHEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Rapid Release Pain Reliever


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