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Ranitidine Hydrochloride - 55111-404-17 - (Ranitidine Hydrochloride)

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Drug Information of Ranitidine Hydrochloride

Product NDC: 55111-404
Proprietary Name: Ranitidine Hydrochloride
Non Proprietary Name: Ranitidine Hydrochloride
Active Ingredient(s): 168    mg/1 & nbsp;   Ranitidine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ranitidine Hydrochloride

Product NDC: 55111-404
Labeler Name: Dr. Reddy's Laboratories Limited
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA078192
Marketing Category: ANDA
Start Marketing Date: 20091202

Package Information of Ranitidine Hydrochloride

Package NDC: 55111-404-17
Package Description: 1 BLISTER PACK in 1 CARTON (55111-404-17) > 8 TABLET, COATED in 1 BLISTER PACK

NDC Information of Ranitidine Hydrochloride

NDC Code 55111-404-17
Proprietary Name Ranitidine Hydrochloride
Package Description 1 BLISTER PACK in 1 CARTON (55111-404-17) > 8 TABLET, COATED in 1 BLISTER PACK
Product NDC 55111-404
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ranitidine Hydrochloride
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20091202
Marketing Category Name ANDA
Labeler Name Dr. Reddy's Laboratories Limited
Substance Name RANITIDINE HYDROCHLORIDE
Strength Number 168
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Ranitidine Hydrochloride


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