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Diphenhydramine Hydrochloride - 53808-0238-1 - (DIPHENHYDRAMINE HYDROCHLORIDE)

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Drug Information of Diphenhydramine Hydrochloride

Product NDC: 53808-0238
Proprietary Name: Diphenhydramine Hydrochloride
Non Proprietary Name: DIPHENHYDRAMINE HYDROCHLORIDE
Active Ingredient(s): 50    mg/1 & nbsp;   DIPHENHYDRAMINE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Diphenhydramine Hydrochloride

Product NDC: 53808-0238
Labeler Name: State of Florida DOH Central Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA080738
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of Diphenhydramine Hydrochloride

Package NDC: 53808-0238-1
Package Description: 30 CAPSULE in 1 BLISTER PACK (53808-0238-1)

NDC Information of Diphenhydramine Hydrochloride

NDC Code 53808-0238-1
Proprietary Name Diphenhydramine Hydrochloride
Package Description 30 CAPSULE in 1 BLISTER PACK (53808-0238-1)
Product NDC 53808-0238
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DIPHENHYDRAMINE HYDROCHLORIDE
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name ANDA
Labeler Name State of Florida DOH Central Pharmacy
Substance Name DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]

Complete Information of Diphenhydramine Hydrochloride


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