United States · FDA National Drug Code directory

Podocon 25

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
71335-2925_c4e909ba-10b5-4c09-afea-4c5d151f657a
Product NDC
71335-2925
Form
TINCTURE
Composition / generic term
Podophyllum resin
Labeler
Bryant Ranch Prepack
Marketing category
UNAPPROVED DRUG OTHER
Marketing start / end (source format)
19900901
Source listing expiry
20261231

Source-listed ingredients

  • PODOPHYLLUM RESIN — 1 mg/4mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE, WITH APPLICATOR in 1 CARTON (71335-2925-1) / 15 mL in 1 BOTTLE, WITH APPLICATOR · 71335-2925-1

Source and coverage

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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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