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Bioelectro Night - 62211-267-24 - (Acetaminophen and Diphenhydramine HCI)

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Drug Information of Bioelectro Night

Product NDC: 62211-267
Proprietary Name: Bioelectro Night
Non Proprietary Name: Acetaminophen and Diphenhydramine HCI
Active Ingredient(s): 500; 25    mg/1; mg/1 & nbsp;   Acetaminophen and Diphenhydramine HCI
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Bioelectro Night

Product NDC: 62211-267
Labeler Name: A&Z Pharmaceutical, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part336
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100930

Package Information of Bioelectro Night

Package NDC: 62211-267-24
Package Description: 1 BOTTLE in 1 BOX (62211-267-24) > 24 TABLET, COATED in 1 BOTTLE

NDC Information of Bioelectro Night

NDC Code 62211-267-24
Proprietary Name Bioelectro Night
Package Description 1 BOTTLE in 1 BOX (62211-267-24) > 24 TABLET, COATED in 1 BOTTLE
Product NDC 62211-267
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen and Diphenhydramine HCI
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100930
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name A&Z Pharmaceutical, Inc.
Substance Name ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 500; 25
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Bioelectro Night


General Information