benzonatate

Product NDC

69499-329

11-digit product format

694990329

Labeler code

69499

Product ID

69499-329_8335a80b-f2d1-4997-8cff-86ffd560de54

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

benzonatate

Dosage form

CAPSULE

Route

ORAL

Labeler

Solubiomix

Application

ANDA040851

Marketing category

ANDA

Marketing start

2017-08-18

Marketing end

2020-11-01

Substance

BENZONATATE

Active strength

150 mg/1

Pharmacologic classes

Decreased Tracheobronchial Stretch Receptor Activity [PE],Non-narcotic Antitussive [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record