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Fexofenadine HCl and Pseudoephedrine HCI - 55111-557-35 - (Fexofenadine HCl and Pseudoephedrine HCI)

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Drug Information of Fexofenadine HCl and Pseudoephedrine HCI

Product NDC: 55111-557
Proprietary Name: Fexofenadine HCl and Pseudoephedrine HCI
Non Proprietary Name: Fexofenadine HCl and Pseudoephedrine HCI
Active Ingredient(s): 180; 240    mg/1; mg/1 & nbsp;   Fexofenadine HCl and Pseudoephedrine HCI
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Fexofenadine HCl and Pseudoephedrine HCI

Product NDC: 55111-557
Labeler Name: Dr.Reddy's Laboratories Limited
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA079043
Marketing Category: ANDA
Start Marketing Date: 20110824

Package Information of Fexofenadine HCl and Pseudoephedrine HCI

Package NDC: 55111-557-35
Package Description: 2 BLISTER PACK in 1 CARTON (55111-557-35) > 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of Fexofenadine HCl and Pseudoephedrine HCI

NDC Code 55111-557-35
Proprietary Name Fexofenadine HCl and Pseudoephedrine HCI
Package Description 2 BLISTER PACK in 1 CARTON (55111-557-35) > 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 55111-557
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Fexofenadine HCl and Pseudoephedrine HCI
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110824
Marketing Category Name ANDA
Labeler Name Dr.Reddy's Laboratories Limited
Substance Name FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 180; 240
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Fexofenadine HCl and Pseudoephedrine HCI


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