Carbidopa and Levodopa

Product NDC
50090-6580
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Carbidopa and Levodopa
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA214092
Marketing category
ANDA
Substance
CARBIDOPA; LEVODOPA
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-6580-190 TABLET in 1 BOTTLE (50090-6580-1) 2023-08-07NoHistorical
50090-6580-2270 TABLET in 1 BOTTLE (50090-6580-2) 2023-08-07NoHistorical
50090-6580-3360 TABLET in 1 BOTTLE (50090-6580-3) 2023-08-07NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Carbidopa and Levodopa Tablets, USPA-S Medication Solutions2023-08-09HUMAN PRESCRIPTION DRUG LABEL2