benzonatate

Product NDC

55154-6849

11-digit product format

551546849

Labeler code

55154

Product ID

55154-6849_1fb20849-07cc-472f-a292-ea01c1edca6d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

benzonatate

Dosage form

CAPSULE

Route

ORAL

Labeler

Cardinal Health

Application

ANDA040627

Marketing category

ANDA

Marketing start

2017-03-22

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