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DIPHENDYDRAMINE HYDROCHLORIDE - 24236-200-24 - (DIPHENDYDRAMINE HYDROCHLORIDE)

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Drug Information of DIPHENDYDRAMINE HYDROCHLORIDE

Product NDC: 24236-200
Proprietary Name: DIPHENDYDRAMINE HYDROCHLORIDE
Non Proprietary Name: DIPHENDYDRAMINE HYDROCHLORIDE
Active Ingredient(s): 25    mg/1 & nbsp;   DIPHENDYDRAMINE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of DIPHENDYDRAMINE HYDROCHLORIDE

Product NDC: 24236-200
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075659
Marketing Category: ANDA
Start Marketing Date: 20101217

Package Information of DIPHENDYDRAMINE HYDROCHLORIDE

Package NDC: 24236-200-24
Package Description: 200 CAPSULE in 1 CANISTER (24236-200-24)

NDC Information of DIPHENDYDRAMINE HYDROCHLORIDE

NDC Code 24236-200-24
Proprietary Name DIPHENDYDRAMINE HYDROCHLORIDE
Package Description 200 CAPSULE in 1 CANISTER (24236-200-24)
Product NDC 24236-200
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DIPHENDYDRAMINE HYDROCHLORIDE
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20101217
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]

Complete Information of DIPHENDYDRAMINE HYDROCHLORIDE


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