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IBUPROFEN AND DIPHENHYDRAMINE HCL - 64380-732-14 - (IBUPROFEN AND DIPHENHYDRAMINE HCL)

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Drug Information of IBUPROFEN AND DIPHENHYDRAMINE HCL

Product NDC: 64380-732
Proprietary Name: IBUPROFEN AND DIPHENHYDRAMINE HCL
Non Proprietary Name: IBUPROFEN AND DIPHENHYDRAMINE HCL
Active Ingredient(s): 25; 200    mg/1; mg/1 & nbsp;   IBUPROFEN AND 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: 64380-732
Labeler Name: Strides Arcolab Limited
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA200888
Marketing Category: ANDA
Start Marketing Date: 20120305

Package Information of IBUPROFEN AND DIPHENHYDRAMINE HCL

Package NDC: 64380-732-14
Package Description: 2 BLISTER PACK in 1 CARTON (64380-732-14) > 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of IBUPROFEN AND DIPHENHYDRAMINE HCL

NDC Code 64380-732-14
Proprietary Name IBUPROFEN AND DIPHENHYDRAMINE HCL
Package Description 2 BLISTER PACK in 1 CARTON (64380-732-14) > 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 64380-732
Product Type Name HUMAN OTC DRUG
Non Proprietary Name IBUPROFEN AND DIPHENHYDRAMINE HCL
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20120305
Marketing Category Name ANDA
Labeler Name Strides Arcolab Limited
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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