CHLORZOXAZONE
Approved
Approval ID
bccfb7cb-f8af-1a85-e053-2a95a90ad052
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Mar 5, 2021
Manufacturers
FDA
Central Packaging
DUNS: 117617671
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 Code80175-0085
Application NumberANDA212254
Product Classification
M
Marketing Category
C73584
G
Generic Name
CHLORZOXAZONE
Product Specifications
Route of AdministrationORAL
Effective DateMarch 5, 2021
FDA Product Classification
INGREDIENTS (1)
CHLORZOXAZONEActive
Quantity: 500 mg in 1 1
Code: H0DE420U8G
Classification: ACTIB