United States · FDA National Drug Code directory

Fludrocortisone acetate

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
72578-164_4b107dc9-d932-49db-87ed-66df936588d7
Product NDC
72578-164
Form
TABLET
Composition / generic term
Fludrocortisone acetate
Labeler
Viona Pharmaceuticals Inc
Marketing category
ANDA
Marketing start / end (source format)
20241202
Source listing expiry
20261231

Source-listed ingredients

  • FLUDROCORTISONE ACETATE — .1 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (72578-164-01) · 72578-164-01
  • 500 TABLET in 1 BOTTLE (72578-164-05) · 72578-164-05

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.

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