Ranitidine
Ranitidine Tablets, USP
Approved
Approval ID
5b9620b9-1660-4b35-b700-6b1347ed9ecb
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 25, 2014
Manufacturers
FDA
RxChange Co.
DUNS: 781126805
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Ranitidine
PRODUCT DETAILS
NDC Product Code33358-316
Application NumberANDA077824
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateNovember 25, 2014
Generic NameRanitidine
INGREDIENTS (1)
RANITIDINE HYDROCHLORIDEActive
Quantity: 150 mg in 1 1
Code: BK76465IHM
Classification: ACTIM