Benzonatate

Product NDC

71335-0054

11-digit product format

713350054

Labeler code

71335

Product ID

71335-0054_930c45c1-a7d3-4eef-809d-7537c1e7945d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Benzonatate

Dosage form

CAPSULE

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA081297

Marketing category

ANDA

Marketing start

2015-06-01

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