Benzonatate

Product NDC

42291-165

11-digit product format

422910165

Labeler code

42291

Product ID

42291-165_62d7f61f-6e60-244c-e053-2991aa0afca5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Benzonatate

Dosage form

CAPSULE, LIQUID FILLED

Route

ORAL

Labeler

AvKARE, Inc.

Application

ANDA040682

Marketing category

ANDA

Marketing start

2016-03-15

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

2020-12-31

Current FDA listing

Historical FDA.report record