Benzonatate

Product NDC

66267-877

11-digit product format

662670877

Labeler code

66267

Product ID

66267-877_9cae2017-ea73-2206-e053-2995a90a82ea

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Benzonatate

Dosage form

CAPSULE

Route

ORAL

Labeler

NuCare Pharmaceuticals,Inc.

Application

ANDA040597

Marketing category

ANDA

Marketing start

2007-04-09

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

2021-12-31

Current FDA listing

Historical FDA.report record