Benzonatate

Product NDC

50090-0872

11-digit product format

500900872

Labeler code

50090

Product ID

50090-0872_94482f28-0d48-49aa-98d6-bec3ab560693

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

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