Benzonatate

Product NDC

55700-363

11-digit product format

557000363

Labeler code

55700

Product ID

55700-363_0e10dc4f-3d67-413f-a1e8-88ee553381b3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Benzonatate

Dosage form

CAPSULE

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA081297

Marketing category

ANDA

Marketing start

2015-06-01

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