benzonatate

Product NDC
63629-1050
11-digit product format
636291050
Labeler code
63629
Product ID
63629-1050_a99e32ea-909a-4cf5-930a-5924238c4881
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
benzonatate
Dosage form
CAPSULE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA040627
Marketing category
ANDA
Marketing start
2017-03-22
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

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63629-1050-163629105001100 CAPSULE in 1 BOTTLE (63629-1050-1) 100 capsule2017-03-220000-00-00NoNoCurrent
63629-1050-26362910500210 CAPSULE in 1 BOTTLE (63629-1050-2) 10 capsule2017-03-220000-00-00NoNoCurrent
63629-1050-36362910500315 CAPSULE in 1 BOTTLE (63629-1050-3) 15 capsule2017-03-220000-00-00NoNoCurrent
63629-1050-46362910500420 CAPSULE in 1 BOTTLE (63629-1050-4) 20 capsule2017-03-220000-00-00NoNoCurrent
63629-1050-56362910500521 CAPSULE in 1 BOTTLE (63629-1050-5) 21 capsule2017-03-220000-00-00NoNoCurrent
63629-1050-66362910500630 CAPSULE in 1 BOTTLE (63629-1050-6) 30 capsule2017-03-220000-00-00NoNoCurrent
63629-1050-763629105007300 CAPSULE in 1 BOTTLE (63629-1050-7) 300 capsule2017-03-220000-00-00NoNoCurrent