# Nystatin

NDC: 0121-0810
Generic name: NYSTATIN
Labeler / Manufacturer: Pharmaceutical Associates, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20160201

FDA application: ANDA203621

## Active ingredients

- NYSTATIN: 100000 [USP'U]/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0121-0810"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0121-0810
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=31e3da10-5a7b-4bc5-8a4f-3e786b64c13a