# Carbidopa-levodopa

NDC: 68002-100
Generic name: carbidopa and levodopa
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250728

FDA application: ANDA216505

## Active ingredients

- CARBIDOPA: 10 mg/1
- LEVODOPA: 100 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68002-100"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68002-100
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dd2215a9-ee0f-443a-a2e3-3d0578c8cd8f