Benzonatate

Product NDC
65841-843
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Benzonatate
Dosage form
CAPSULE
Route
ORAL
Labeler
Zydus Lifesciences Limited
Application
ANDA040597
Marketing category
ANDA
Substance
BENZONATATE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
65841-843-01100 CAPSULE in 1 BOTTLE (65841-843-01) 2007-09-04NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Benzonatate Capsules, USPZydus Lifesciences Limited2024-11-25HUMAN PRESCRIPTION DRUG LABEL9