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
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code33358-316
Application NumberANDA077824
Product Classification
M
Marketing Category
C73584
G
Generic Name
Ranitidine
Product Specifications
Route of AdministrationORAL
Effective DateNovember 25, 2014
FDA Product Classification
INGREDIENTS (1)
RANITIDINE HYDROCHLORIDEActive
Quantity: 150 mg in 1 1
Code: BK76465IHM
Classification: ACTIM