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Ibuprofen and Diphenhydramine Citrate - 55111-565-40 - (Ibuprofen and Diphenhydramine Citrate)

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Drug Information of Ibuprofen and Diphenhydramine Citrate

Product NDC: 55111-565
Proprietary Name: Ibuprofen and Diphenhydramine Citrate
Non Proprietary Name: Ibuprofen and Diphenhydramine Citrate
Active Ingredient(s): 38; 200    mg/1; mg/1 & nbsp;   Ibuprofen and Diphenhydramine Citrate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Ibuprofen and Diphenhydramine Citrate

Product NDC: 55111-565
Labeler Name: Dr. Reddy's Laboratories Limited
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA090619
Marketing Category: ANDA
Start Marketing Date: 20100131

Package Information of Ibuprofen and Diphenhydramine Citrate

Package NDC: 55111-565-40
Package Description: 1 BOTTLE in 1 CARTON (55111-565-40) > 40 TABLET in 1 BOTTLE

NDC Information of Ibuprofen and Diphenhydramine Citrate

NDC Code 55111-565-40
Proprietary Name Ibuprofen and Diphenhydramine Citrate
Package Description 1 BOTTLE in 1 CARTON (55111-565-40) > 40 TABLET in 1 BOTTLE
Product NDC 55111-565
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen and Diphenhydramine Citrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100131
Marketing Category Name ANDA
Labeler Name Dr. Reddy's Laboratories Limited
Substance Name DIPHENHYDRAMINE CITRATE; IBUPROFEN
Strength Number 38; 200
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Ibuprofen and Diphenhydramine Citrate


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