Benzonatate

Product NDC

68788-7014

11-digit product format

687887014

Labeler code

68788

Product ID

68788-7014_ee2598f3-f615-4fdd-913d-f19f5877b1de

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Benzonatate

Dosage form

CAPSULE

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA091133

Marketing category

ANDA

Marketing start

2017-08-29

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