Benzonatate

Product NDC

68788-9827

11-digit product format

687889827

Labeler code

68788

Product ID

68788-9827_9933a7fa-5473-4ff4-ab00-55ca02f7c6d3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Benzonatate

Dosage form

CAPSULE, LIQUID FILLED

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA040682

Marketing category

ANDA

Marketing start

2012-04-05

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

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record