RANITIDINE
RANITIDINE
Approved
Approval ID
fd4d06b3-8fd9-49f4-9dcb-0a57386fe4de
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 10, 2014
Manufacturers
FDA
Northwind Pharmaceuticals, LLC
DUNS: 036986393
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
ranitidine hydrochloride
PRODUCT DETAILS
NDC Product Code51655-681
Application NumberANDA077824
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateNovember 10, 2014
Generic Nameranitidine hydrochloride
INGREDIENTS (1)
RANITIDINE HYDROCHLORIDEActive
Quantity: 150 mg in 1 1
Code: BK76465IHM
Classification: ACTIM