Ranitidine - 55111-602-16 - (Ranitidine)

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Drug Information of Ranitidine

Product NDC: 55111-602
Proprietary Name: Ranitidine
Non Proprietary Name: Ranitidine
Active Ingredient(s): 15    mg/mL & nbsp;   Ranitidine
Administration Route(s): ORAL
Dosage Form(s): SYRUP
Coding System: National Drug Codes(NDC)

Labeler Information of Ranitidine

Product NDC: 55111-602
Labeler Name: Dr. Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090102
Marketing Category: ANDA
Start Marketing Date: 20090526

Package Information of Ranitidine

Package NDC: 55111-602-16
Package Description: 480 mL in 1 BOTTLE (55111-602-16)

NDC Information of Ranitidine

NDC Code 55111-602-16
Proprietary Name Ranitidine
Package Description 480 mL in 1 BOTTLE (55111-602-16)
Product NDC 55111-602
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ranitidine
Dosage Form Name SYRUP
Route Name ORAL
Start Marketing Date 20090526
Marketing Category Name ANDA
Labeler Name Dr. Reddy's Laboratories Limited
Substance Name RANITIDINE HYDROCHLORIDE
Strength Number 15
Strength Unit mg/mL
Pharmaceutical Classes Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

Complete Information of Ranitidine


General Information