Ranitidine - 0603-9418-56 - (Ranitidine)

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Drug Information of Ranitidine

Product NDC: 0603-9418
Proprietary Name: Ranitidine
Non Proprietary Name: Ranitidine
Active Ingredient(s): 75    mg/5mL & nbsp;   Ranitidine
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ranitidine

Product NDC: 0603-9418
Labeler Name: Qualitest Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078890
Marketing Category: ANDA
Start Marketing Date: 20100701

Package Information of Ranitidine

Package NDC: 0603-9418-56
Package Description: 237 mL in 1 BOTTLE (0603-9418-56)

NDC Information of Ranitidine

NDC Code 0603-9418-56
Proprietary Name Ranitidine
Package Description 237 mL in 1 BOTTLE (0603-9418-56)
Product NDC 0603-9418
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ranitidine
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20100701
Marketing Category Name ANDA
Labeler Name Qualitest Pharmaceuticals
Substance Name RANITIDINE HYDROCHLORIDE
Strength Number 75
Strength Unit mg/5mL
Pharmaceutical Classes Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

Complete Information of Ranitidine


General Information