# Duopa

NDC: 0074-3012
Generic name: Carbidopa and Levodopa
Labeler / Manufacturer: AbbVie Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SUSPENSION
Routes: ENTERAL
Marketing started: 20150115

FDA application: NDA203952

## Active ingredients

- CARBIDOPA HYDRATE: 4.63 mg/mL
- LEVODOPA: 20 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0074-3012"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0074-3012
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7066d371-dc6a-0d6f-7bed-e5dd4ee912da