Benzonatate

Product NDC

70518-0837

11-digit product format

705180837

Labeler code

70518

Product ID

70518-0837_8edf0b6b-df24-919e-e053-2a95a90a5182

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Benzonatate

Dosage form

CAPSULE, LIQUID FILLED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA040682

Marketing category

ANDA

Marketing start

2017-11-10

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