Benzonatate

Product NDC
71205-662
11-digit product format
712050662
Labeler code
71205
Product ID
71205-662_ca7f3bd7-fa5d-441a-9b9b-5329349c3e98
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Benzonatate
Dosage form
CAPSULE
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA091310
Marketing category
ANDA
Marketing start
2021-08-02
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
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71205-662-30EA - Each71205-66203c597d0-426f-480f-8b53-f53ce5aa6b1312022-08-04

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71205-662BENZONATATE CAPSULE [PROFICIENT RX LP]1Legacy NDC20220521_ca7f3bd7-fa5d-441a-9b9b-5329349c3e98.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71205-662-107120506621010 CAPSULE in 1 BOTTLE (71205-662-10) 10 capsule2022-05-200000-00-00NoNoCurrent
71205-662-147120506621414 CAPSULE in 1 BOTTLE (71205-662-14) 14 capsule2022-05-200000-00-00NoNoCurrent
71205-662-157120506621515 CAPSULE in 1 BOTTLE (71205-662-15) 15 capsule2022-05-200000-00-00NoNoCurrent
71205-662-207120506622020 CAPSULE in 1 BOTTLE (71205-662-20) 20 capsule2022-05-200000-00-00NoNoCurrent
71205-662-307120506623030 CAPSULE in 1 BOTTLE (71205-662-30) 30 capsule2022-05-200000-00-00NoNoCurrent
71205-662-607120506626060 CAPSULE in 1 BOTTLE (71205-662-60) 60 capsule2022-05-200000-00-00NoNoCurrent
71205-662-907120506629090 CAPSULE in 1 BOTTLE (71205-662-90) 90 capsule2022-05-200000-00-00NoNoCurrent