United States · FDA National Drug Code directory

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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
71399-8460_42b7c75d-d66d-77f9-e063-6294a90a4e40
Product NDC
71399-8460
Form
SUPPOSITORY
Composition / generic term
BISACODYL
Labeler
AKRON PHARMA INC
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20240913
Source listing expiry
20261231

Source-listed ingredients

  • BISACODYL — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 12 BLISTER PACK in 1 BOX (71399-8460-2) / 1 SUPPOSITORY in 1 BLISTER PACK · 71399-8460-2
  • 50 BLISTER PACK in 1 BOX (71399-8460-5) / 1 SUPPOSITORY in 1 BLISTER PACK · 71399-8460-5

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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