# CYSTADROPS

NDC: 55292-410
Generic name: cysteamine hydrochloride
Labeler / Manufacturer: RECORDATI RARE DISEASES, INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SOLUTION
Routes: OPHTHALMIC
Marketing started: 20200819

FDA application: NDA211302

## Active ingredients

- CYSTEAMINE HYDROCHLORIDE: 3.5 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55292-410"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55292-410
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5d2bcce3-9b89-4141-aeb7-db00449047f5