benzonatate

Product NDC

0440-7186

11-digit product format

004407186

Labeler code

0440

Product ID

0440-7186_58e759cf-f686-453c-9575-91f74b00350a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

benzonatate

Dosage form

CAPSULE

Route

ORAL

Labeler

Liberty Pharmaceuticals, Inc.

Application

ANDA040749

Marketing category

ANDA

Marketing start

2007-07-25

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

2020-12-31

Current FDA listing

Historical FDA.report record