Chlorzoxazone
Chlorzoxazone Tablets, USP 500 mg
Approved
Approval ID
7c6c02a1-1774-4332-babd-dff86f9638a0
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 12, 2024
Manufacturers
FDA
Bryant Ranch Prepack
DUNS: 171714327
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Chlorzoxazone
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code63629-9158
Application NumberANDA212254
Product Classification
M
Marketing Category
C73584
G
Generic Name
Chlorzoxazone
Product Specifications
Route of AdministrationORAL
Effective DateMarch 26, 2020
FDA Product Classification
INGREDIENTS (1)
CHLORZOXAZONEActive
Quantity: 500 mg in 1 1
Code: H0DE420U8G
Classification: ACTIB