Benzonatate

Product NDC
0615-7678
11-digit product format
006157678
Labeler code
0615
Product ID
0615-7678_5477b3da-5999-430b-815b-394cfd786d19
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Benzonatate
Dosage form
CAPSULE
Route
ORAL
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Application
ANDA040597
Marketing category
ANDA
Marketing start
2007-09-04
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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0615-7678-392021-03-17C16284748780-197449f38-d337-f6ea-e053-dbdaa90aa70303fb833b-a334-4ad2-8849-0336782d8b79
0615-7678-392019-11-13C16284748780-197449f38-d337-f6ea-e053-dbdaa90aa70303fb833b-a334-4ad2-8849-0336782d8b79