Benzonatate
BENZONATATE capsule, liquid filled
Approved
Approval ID
222b9299-255c-44b4-9b7a-b9e16e36fe99
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 27, 2009
Manufacturers
FDA
Stat Rx USA
DUNS: 786036330
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 Code16590-031
Application NumberANDA040682
Product Classification
M
Marketing Category
C73584
G
Generic Name
Benzonatate
Product Specifications
Route of AdministrationORAL
Effective DateOctober 27, 2009
FDA Product Classification
INGREDIENTS (1)
BenzonatateActive
Quantity: 100 mg in 1 1
Code: 5P4DHS6ENR
Classification: ACTIB