United States · FDA National Drug Code directory

NYSTATIN

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
81033-015_50738a43-7297-270c-e063-6294a90af2cc
Product NDC
81033-015
Form
SUSPENSION
Composition / generic term
NYSTATIN
Labeler
Kesin Pharma Corporation
Marketing category
ANDA
Marketing start / end (source format)
20200814
Source listing expiry
20271231

Source-listed ingredients

  • NYSTATIN — 100000 U/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 473 mL in 1 BOTTLE (81033-015-16) · 81033-015-16
  • 1 BOTTLE in 1 CARTON (81033-015-60) / 60 mL in 1 BOTTLE · 81033-015-60

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →