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Ibuprofen and Pseudoephedrine Hydrochloride - 0363-0423-41 - (Ibuprofen and Pseudoephedrine Hydrochloride)

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Drug Information of Ibuprofen and Pseudoephedrine Hydrochloride

Product NDC: 0363-0423
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, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ibuprofen and Pseudoephedrine Hydrochloride

Product NDC: 0363-0423
Labeler Name: Walgreen Company
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074567
Marketing Category: ANDA
Start Marketing Date: 20011008

Package Information of Ibuprofen and Pseudoephedrine Hydrochloride

Package NDC: 0363-0423-41
Package Description: 40 TABLET, COATED in 1 BLISTER PACK (0363-0423-41)

NDC Information of Ibuprofen and Pseudoephedrine Hydrochloride

NDC Code 0363-0423-41
Proprietary Name Ibuprofen and Pseudoephedrine Hydrochloride
Package Description 40 TABLET, COATED in 1 BLISTER PACK (0363-0423-41)
Product NDC 0363-0423
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen and Pseudoephedrine Hydrochloride
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20011008
Marketing Category Name ANDA
Labeler Name Walgreen Company
Substance Name IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 200; 30
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Ibuprofen and Pseudoephedrine Hydrochloride


General Information