Carbidopa and Levodopa

Product NDC
50090-7499
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Carbidopa and Levodopa
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA216537
Marketing category
ANDA
Substance
CARBIDOPA; LEVODOPA
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-7499-090 TABLET in 1 BOTTLE (50090-7499-0) 2025-01-21NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Carbidopa and Levodopa Tablets, USP R X onlyA-S Medication Solutions2025-01-22Human Prescription Drug Label1