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Fexofenadine hydrochloride - 55111-784-29 - (Fexofenadine hydrochloride)

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Drug Information of Fexofenadine hydrochloride

Product NDC: 55111-784
Proprietary Name: Fexofenadine hydrochloride
Non Proprietary Name: Fexofenadine hydrochloride
Active Ingredient(s): 180    mg/1 & nbsp;   Fexofenadine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Fexofenadine hydrochloride

Product NDC: 55111-784
Labeler Name: Dr. Reddy's Laboratories Limited
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076502
Marketing Category: ANDA
Start Marketing Date: 20110415

Package Information of Fexofenadine hydrochloride

Package NDC: 55111-784-29
Package Description: 3 BLISTER PACK in 1 CARTON (55111-784-29) > 5 TABLET in 1 BLISTER PACK

NDC Information of Fexofenadine hydrochloride

NDC Code 55111-784-29
Proprietary Name Fexofenadine hydrochloride
Package Description 3 BLISTER PACK in 1 CARTON (55111-784-29) > 5 TABLET in 1 BLISTER PACK
Product NDC 55111-784
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Fexofenadine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110415
Marketing Category Name ANDA
Labeler Name Dr. Reddy's Laboratories Limited
Substance Name FEXOFENADINE HYDROCHLORIDE
Strength Number 180
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Fexofenadine hydrochloride


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