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Headache Relief PM - 55910-373-15 - (Acetaminophen and Diphenhydramine Citrate)

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Drug Information of Headache Relief PM

Product NDC: 55910-373
Proprietary Name: Headache Relief PM
Non Proprietary Name: Acetaminophen and Diphenhydramine Citrate
Active Ingredient(s): 500; 38    mg/1; mg/1 & nbsp;   Acetaminophen and Diphenhydramine Citrate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Headache Relief PM

Product NDC: 55910-373
Labeler Name: DOLGENCORP, LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part338
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20040607

Package Information of Headache Relief PM

Package NDC: 55910-373-15
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (55910-373-15) > 50 TABLET in 1 BOTTLE, PLASTIC

NDC Information of Headache Relief PM

NDC Code 55910-373-15
Proprietary Name Headache Relief PM
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (55910-373-15) > 50 TABLET in 1 BOTTLE, PLASTIC
Product NDC 55910-373
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen and Diphenhydramine Citrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040607
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name DOLGENCORP, LLC
Substance Name ACETAMINOPHEN; DIPHENHYDRAMINE CITRATE
Strength Number 500; 38
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Headache Relief PM


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