Carbidopa and Levodopa

Product NDC
72162-2193
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Carbidopa and Levodopa
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA214091
Marketing category
ANDA
Substance
CARBIDOPA; LEVODOPA
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
72162-2193-1100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2193-1) 2023-12-15NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Carbidopa and Levodopa Extended-Release Tablets, USP Rx onlyBryant Ranch Prepack2023-12-15HUMAN PRESCRIPTION DRUG LABEL101