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Ibuprofen and Pseudoephedrine hydrochloride - 51660-423-41 - (ibuprofen and pseudoephedrine hydrochloride)

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Drug Information of Ibuprofen and Pseudoephedrine hydrochloride

Product NDC: 51660-423
Proprietary Name: Ibuprofen and Pseudoephedrine hydrochloride
Non Proprietary Name: ibuprofen and pseudoephedrine hydrochloride
Active Ingredient(s): 200; 30    mg/1; mg/1 & nbsp;   ibuprofen and pseudoephedrine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, SUGAR COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ibuprofen and Pseudoephedrine hydrochloride

Product NDC: 51660-423
Labeler Name: Ohm Laboratories Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074567
Marketing Category: ANDA
Start Marketing Date: 20011013

Package Information of Ibuprofen and Pseudoephedrine hydrochloride

Package NDC: 51660-423-41
Package Description: 40 TABLET, SUGAR COATED in 1 BLISTER PACK (51660-423-41)

NDC Information of Ibuprofen and Pseudoephedrine hydrochloride

NDC Code 51660-423-41
Proprietary Name Ibuprofen and Pseudoephedrine hydrochloride
Package Description 40 TABLET, SUGAR COATED in 1 BLISTER PACK (51660-423-41)
Product NDC 51660-423
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ibuprofen and pseudoephedrine hydrochloride
Dosage Form Name TABLET, SUGAR COATED
Route Name ORAL
Start Marketing Date 20011013
Marketing Category Name ANDA
Labeler Name Ohm Laboratories Inc.
Substance Name IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 200; 30
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Ibuprofen and Pseudoephedrine hydrochloride


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