Ranitidine - 55390-616-01 - (Ranitidine hydrochloride)

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Drug Information of Ranitidine

Product NDC: 55390-616
Proprietary Name: Ranitidine
Non Proprietary Name: Ranitidine hydrochloride
Active Ingredient(s): 25    mg/mL & nbsp;   Ranitidine hydrochloride
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ranitidine

Product NDC: 55390-616
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074777
Marketing Category: ANDA
Start Marketing Date: 20041119

Package Information of Ranitidine

Package NDC: 55390-616-01
Package Description: 1 VIAL in 1 BOX (55390-616-01) > 6 mL in 1 VIAL

NDC Information of Ranitidine

NDC Code 55390-616-01
Proprietary Name Ranitidine
Package Description 1 VIAL in 1 BOX (55390-616-01) > 6 mL in 1 VIAL
Product NDC 55390-616
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ranitidine hydrochloride
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20041119
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
Substance Name RANITIDINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/mL
Pharmaceutical Classes Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

Complete Information of Ranitidine


General Information