Benzonatate

Product NDC
66267-033
11-digit product format
662670033
Labeler code
66267
Product ID
66267-033_9cafd6c6-c16a-8044-e053-2a95a90aecab
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Benzonatate
Dosage form
CAPSULE
Route
ORAL
Labeler
NuCare Pharmaceuticals, Inc.
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
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
66267-033-15EA - Each66267-033a18b3766-8e6e-4bbf-9b44-3a3dc2ef838f12016-10-06
66267-033-20EA - Each66267-03398279ad8-6c3a-466a-81d7-60aea030391b12016-10-06
66267-033-30EA - Each66267-0334719f1b0-93ad-4561-919d-910337e596f012016-10-06