Benzonatate

Product NDC
71205-699
11-digit product format
712050699
Labeler code
71205
Product ID
71205-699_47560d98-f4c4-4738-85fe-41cbed09ed59
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Benzonatate
Dosage form
CAPSULE
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA211518
Marketing category
ANDA
Marketing start
2019-02-22
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
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
5P4DHS6ENRBENZONATATE104-31-4BENZONATATE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71205-699-107120506991010 CAPSULE in 1 BOTTLE (71205-699-10) 10 capsule2022-09-16NoNoHistorical
71205-699-147120506991414 CAPSULE in 1 BOTTLE (71205-699-14) 14 capsule2022-09-16NoNoHistorical
71205-699-207120506992020 CAPSULE in 1 BOTTLE (71205-699-20) 20 capsule2022-09-16NoNoHistorical
71205-699-217120506992121 CAPSULE in 1 BOTTLE (71205-699-21) 21 capsule2022-09-16NoNoHistorical
71205-699-247120506992424 CAPSULE in 1 BOTTLE (71205-699-24) 24 capsule2022-09-16NoNoHistorical
71205-699-307120506993030 CAPSULE in 1 BOTTLE (71205-699-30) 30 capsule2022-09-16NoNoHistorical
71205-699-607120506996060 CAPSULE in 1 BOTTLE (71205-699-60) 60 capsule2022-09-16NoNoHistorical
71205-699-907120506999090 CAPSULE in 1 BOTTLE (71205-699-90) 90 capsule2022-09-16NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
BENZONATATE CAPSULES 100 mg Capsules (benzonatate, USP)Proficient Rx LP2022-09-01HUMAN PRESCRIPTION DRUG LABEL1