Ranitidine - 53808-0774-1 - (Ranitidine)

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Drug Information of Ranitidine

Product NDC: 53808-0774
Proprietary Name: Ranitidine
Non Proprietary Name: Ranitidine
Active Ingredient(s): 150    mg/1 & nbsp;   Ranitidine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Ranitidine

Product NDC: 53808-0774
Labeler Name: State of Florida DOH Central Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075180
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of Ranitidine

Package NDC: 53808-0774-1
Package Description: 30 TABLET in 1 BLISTER PACK (53808-0774-1)

NDC Information of Ranitidine

NDC Code 53808-0774-1
Proprietary Name Ranitidine
Package Description 30 TABLET in 1 BLISTER PACK (53808-0774-1)
Product NDC 53808-0774
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ranitidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name ANDA
Labeler Name State of Florida DOH Central Pharmacy
Substance Name RANITIDINE
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

Complete Information of Ranitidine


General Information