# NYSTATIN

NDC: 17856-0508
Generic name: NYSTATIN
Labeler / Manufacturer: ATLANTIC BIOLOGICALS CORP.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20221205

FDA application: ANDA214346

## 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:"17856-0508"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=17856-0508
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5c08148f-83e5-4f14-b0d3-af8d2c26062e