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pain relief - 49738-010-78 - (Acetaminophen)

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Drug Information of pain relief

Product NDC: 49738-010
Proprietary Name: 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 pain relief

Product NDC: 49738-010
Labeler Name: Kmart Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20050309

Package Information of pain relief

Package NDC: 49738-010-78
Package Description: 1 BOTTLE in 1 CARTON (49738-010-78) > 100 TABLET, COATED in 1 BOTTLE

NDC Information of pain relief

NDC Code 49738-010-78
Proprietary Name pain relief
Package Description 1 BOTTLE in 1 CARTON (49738-010-78) > 100 TABLET, COATED in 1 BOTTLE
Product NDC 49738-010
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20050309
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Kmart Corporation
Substance Name ACETAMINOPHEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of pain relief


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