# Carbidopa and Levodopa

NDC: 75907-022
Generic name: Carbidopa and Levodopa
Labeler / Manufacturer: Dr. Reddy's Laboratories Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20240501

FDA application: ANDA073618

## Active ingredients

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

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"75907-022"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=75907-022
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=87ab55c9-203d-d595-3e3e-0e38f2f6d9c4