Benzonatate

Product NDC

63629-2655

11-digit product format

636292655

Labeler code

63629

Product ID

63629-2655_ccb3093d-1b48-4c18-bb54-83e72b7c7b12

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Benzonatate

Dosage form

CAPSULE

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA081297

Marketing category

ANDA

Marketing start

1993-04-01

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

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record