Benzonatate

Product NDC

0615-1349

11-digit product format

006151349

Labeler code

0615

Product ID

0615-1349_af8036bf-eecc-4e91-a66c-e6bf5dbb8f79

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Benzonatate

Dosage form

CAPSULE

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

ANDA081297

Marketing category

ANDA

Marketing start

2010-11-14

Marketing end

0000-00-00

Substance

BENZONATATE

Active strength

100 mg/1

Pharmacologic classes

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

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record