benzonatate

Product NDC

60760-051

11-digit product format

607600051

Labeler code

60760

Product ID

60760-051_7a02d090-1e22-c462-e053-2991aa0a8a67

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

benzonatate

Dosage form

CAPSULE

Route

ORAL

Labeler

St Marys Medical Park Pharmacy

Application

ANDA040627

Marketing category

ANDA

Marketing start

2007-07-25

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

2020-12-31

Current FDA listing

Historical FDA.report record