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Ibuprofen and Diphenhydramine HCl - 68016-217-16 - (IBUPROFEN, DIPHENHYDRAMINE HCL)

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Drug Information of Ibuprofen and Diphenhydramine HCl

Product NDC: 68016-217
Proprietary Name: Ibuprofen and Diphenhydramine HCl
Non Proprietary Name: IBUPROFEN, DIPHENHYDRAMINE HCL
Active Ingredient(s): 25; 200    mg/1; mg/1 & nbsp;   IBUPROFEN, DIPHENHYDRAMINE HCL
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Ibuprofen and Diphenhydramine HCl

Product NDC: 68016-217
Labeler Name: Premier Value (Chain Drug Consortium, LLC)
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA090397
Marketing Category: ANDA
Start Marketing Date: 20130104

Package Information of Ibuprofen and Diphenhydramine HCl

Package NDC: 68016-217-16
Package Description: 1 BOTTLE in 1 BOX (68016-217-16) > 16 CAPSULE, LIQUID FILLED in 1 BOTTLE

NDC Information of Ibuprofen and Diphenhydramine HCl

NDC Code 68016-217-16
Proprietary Name Ibuprofen and Diphenhydramine HCl
Package Description 1 BOTTLE in 1 BOX (68016-217-16) > 16 CAPSULE, LIQUID FILLED in 1 BOTTLE
Product NDC 68016-217
Product Type Name HUMAN OTC DRUG
Non Proprietary Name IBUPROFEN, DIPHENHYDRAMINE HCL
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20130104
Marketing Category Name ANDA
Labeler Name Premier Value (Chain Drug Consortium, LLC)
Substance Name DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN
Strength Number 25; 200
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Ibuprofen and Diphenhydramine HCl


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