benzonatate

Product NDC

63739-124

11-digit product format

637390124

Labeler code

63739

Product ID

63739-124_d29960e1-e11f-4ae4-b904-25133937076d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

benzonatate

Dosage form

CAPSULE

Route

ORAL

Labeler

McKesson Corporation

Application

ANDA040749

Marketing category

ANDA

Marketing start

2017-03-22

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