Ranitidine - 54838-550-80 - (Ranitidine Hydrochloride)

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Drug Information of Ranitidine

Product NDC: 54838-550
Proprietary Name: Ranitidine
Non Proprietary Name: Ranitidine Hydrochloride
Active Ingredient(s): 15    mg/mL & nbsp;   Ranitidine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ranitidine

Product NDC: 54838-550
Labeler Name: Silarx Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091288
Marketing Category: ANDA
Start Marketing Date: 20101210

Package Information of Ranitidine

Package NDC: 54838-550-80
Package Description: 473 mL in 1 BOTTLE, PLASTIC (54838-550-80)

NDC Information of Ranitidine

NDC Code 54838-550-80
Proprietary Name Ranitidine
Package Description 473 mL in 1 BOTTLE, PLASTIC (54838-550-80)
Product NDC 54838-550
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ranitidine Hydrochloride
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20101210
Marketing Category Name ANDA
Labeler Name Silarx Pharmaceuticals, Inc
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