# Carbidopa

NDC: 16714-067
Generic name: Carbidopa
Labeler / Manufacturer: NorthStar Rx LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20191021

FDA application: ANDA211055

## Active ingredients

- CARBIDOPA: 25 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"16714-067"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16714-067
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=33ee4598-cbcc-45e0-a48e-dc0101e1f204