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Rx Act Pain Relief - 37808-046-83 - (Acetaminophen)

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Drug Information of Rx Act Pain Relief

Product NDC: 37808-046
Proprietary Name: Rx Act Pain Relief
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 500    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Rx Act Pain Relief

Product NDC: 37808-046
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100201

Package Information of Rx Act Pain Relief

Package NDC: 37808-046-83
Package Description: 225 TABLET, COATED in 1 BOTTLE (37808-046-83)

NDC Information of Rx Act Pain Relief

NDC Code 37808-046-83
Proprietary Name Rx Act Pain Relief
Package Description 225 TABLET, COATED in 1 BOTTLE (37808-046-83)
Product NDC 37808-046
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20100201
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name H E B
Substance Name ACETAMINOPHEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Rx Act Pain Relief


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