Nizatidine
Nizatidine Insert & Label
Approved
Approval ID
e133d726-2a1f-4f9a-96b3-320f5cd9f7b0
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 14, 2010
Manufacturers
FDA
nizatidine
DUNS: 786036330
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
nizatidine
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code16590-741
Application NumberANDA076178
Product Classification
M
Marketing Category
C73584
G
Generic Name
nizatidine
Product Specifications
Route of AdministrationORAL
Effective DateJanuary 14, 2010
FDA Product Classification
INGREDIENTS (1)
NizatidineActive
Quantity: 150 mg in 1 1
Code: P41PML4GHR
Classification: ACTIB