# Carbidopa and Levodopa

NDC: 60687-836
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: 20240316

FDA application: ANDA074260

## Active ingredients

- CARBIDOPA: 25 mg/1
- LEVODOPA: 250 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60687-836"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60687-836
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a62ae74d-6677-459c-b338-00e6851a1e00