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rx act pain relief pm - 37808-829-60 - (Acetaminophen, Diphenhydramine HCl)

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Drug Information of rx act pain relief pm

Product NDC: 37808-829
Proprietary Name: rx act pain relief pm
Non Proprietary Name: Acetaminophen, Diphenhydramine HCl
Active Ingredient(s): 500; 25    mg/1; mg/1 & nbsp;   Acetaminophen, Diphenhydramine HCl
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of rx act pain relief pm

Product NDC: 37808-829
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: part338
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100826

Package Information of rx act pain relief pm

Package NDC: 37808-829-60
Package Description: 1 BOTTLE in 1 CARTON (37808-829-60) > 20 CAPSULE, COATED in 1 BOTTLE

NDC Information of rx act pain relief pm

NDC Code 37808-829-60
Proprietary Name rx act pain relief pm
Package Description 1 BOTTLE in 1 CARTON (37808-829-60) > 20 CAPSULE, COATED in 1 BOTTLE
Product NDC 37808-829
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Diphenhydramine HCl
Dosage Form Name CAPSULE, COATED
Route Name ORAL
Start Marketing Date 20100826
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name H E B
Substance Name ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 500; 25
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of rx act pain relief pm


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