Benzonatate

Product NDC

50090-0532

11-digit product format

500900532

Labeler code

50090

Product ID

50090-0532_bf076a98-29b8-4ba0-b3a6-13d114f35b61

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Benzonatate

Dosage form

CAPSULE, LIQUID FILLED

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA040682

Marketing category

ANDA

Marketing start

2010-06-04

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