benzonatate

Product NDC

68071-3185

11-digit product format

680713185

Labeler code

68071

Product ID

68071-3185_4b442214-c3d0-2a3a-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

benzonatate

Dosage form

CAPSULE

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA040749

Marketing category

ANDA

Marketing start

2007-07-25

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