OXAZEPAM
Approved
Approval ID
a70c61ac-412c-4886-9c5e-7b7e5d84fbb5
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 15, 2009
Manufacturers
FDA
STAT RX USA LLC
DUNS: 786036330
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
OXAZEPAM
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code16590-304
Application NumberANDA072252
Product Classification
M
Marketing Category
C73584
G
Generic Name
OXAZEPAM
Product Specifications
Route of AdministrationORAL
Effective DateDecember 15, 2009
FDA Product Classification
INGREDIENTS (1)
OXAZEPAMActive
Quantity: 15 mg in 1 1
Code: 6GOW6DWN2A
Classification: ACTIB