Benzonatate

Product NDC

42708-015

11-digit product format

427080015

Labeler code

42708

Product ID

42708-015_c8c45ea2-efd7-4cff-bb36-f2d4b9611bb1

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Benzonatate

Dosage form

CAPSULE, LIQUID FILLED

Route

ORAL

Labeler

QPharma Inc

Application

ANDA040682

Marketing category

ANDA

Marketing start

2010-06-04

Marketing end

0000-00-00

Substance

BENZONATATE

Active strength

200 mg/1

Pharmacologic classes

Decreased Tracheobronchial Stretch Receptor Activity [PE],Non-narcotic Antitussive [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record