Benzonatate

Product NDC
72162-1561
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Benzonatate
Dosage form
CAPSULE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA202765
Marketing category
ANDA
Substance
BENZONATATE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
72162-1561-1100 CAPSULE in 1 BOTTLE (72162-1561-1) 2023-08-29NoHistorical
72162-1561-5500 CAPSULE in 1 BOTTLE (72162-1561-5) 2023-08-29NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Benzonatate Capsules USP, 100 mg and 200 mgBryant Ranch Prepack2023-08-29HUMAN PRESCRIPTION DRUG LABEL101