Ranitidine
Ranitidine Tablets, USP
Approved
Approval ID
a9fef8f6-b823-4b8a-84b8-2b916374adb5
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 17, 2009
Manufacturers
FDA
Rebel Distributors
DUNS: 118802834
Products 2
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 Code21695-110
Application NumberANDA077824
Product Classification
M
Marketing Category
C73584
G
Generic Name
Ranitidine
Product Specifications
Route of AdministrationORAL
Effective DateDecember 17, 2009
FDA Product Classification
INGREDIENTS (1)
RANITIDINE HYDROCHLORIDEActive
Quantity: 300 mg in 1 1
Code: BK76465IHM
Classification: ACTIB
Ranitidine
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code21695-109
Application NumberANDA077824
Product Classification
M
Marketing Category
C73584
G
Generic Name
Ranitidine
Product Specifications
Route of AdministrationORAL
Effective DateDecember 17, 2009
FDA Product Classification
INGREDIENTS (1)
RANITIDINE HYDROCHLORIDEActive
Quantity: 150 mg in 1 1
Code: BK76465IHM
Classification: ACTIB