Carbidopa and Levodopa

Product NDC
50090-7186
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
50090-7186-030 TABLET in 1 BOTTLE (50090-7186-0) 2024-06-26NoHistorical
50090-7186-190 TABLET in 1 BOTTLE (50090-7186-1) 2024-06-26NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Carbidopa and Levodopa Tablets, USP Rx onlyA-S Medication Solutions2024-06-28HUMAN PRESCRIPTION DRUG LABEL4