BENZONATATE
Benzonatate
Approved
Approval ID
9bbd5a37-2bc4-4522-af21-67719f98d97c
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 30, 2015
Manufacturers
FDA
Northwind Pharmaceuticals, LLC
DUNS: 036986393
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
BENZONATATE
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code51655-769
Application NumberANDA040627
Product Classification
M
Marketing Category
C73584
G
Generic Name
BENZONATATE
Product Specifications
Route of AdministrationORAL
Effective DateOctober 30, 2015
FDA Product Classification
INGREDIENTS (1)
BENZONATATEActive
Quantity: 100 mg in 1 1
Code: 5P4DHS6ENR
Classification: ACTIB