benzonatate

Product NDC
43063-111
11-digit product format
430630111
Labeler code
43063
Product ID
43063-111_7d672662-7ab7-8d7b-e053-2a91aa0aa658
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
benzonatate
Dosage form
CAPSULE
Route
ORAL
Labeler
PD-Rx Pharmaceuticals, Inc.
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
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
43063-111-04EA - Each43063-1116ad0822b-3435-4fa2-a7b2-7f72ea1d5c7612013-08-02
43063-111-06EA - Each43063-111bff1f304-659e-49b6-abfb-278240bca42b12012-07-24