benzonatate

Product NDC

50090-0534

11-digit product format

500900534

Labeler code

50090

Product ID

50090-0534_b4faa752-aec5-43e5-bbd5-779dc1806430

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

benzonatate

Dosage form

CAPSULE

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA040627

Marketing category

ANDA

Marketing start

2007-07-25

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