United States · FDA National Drug Code directory

Biotin

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
87492-002_4c6ec616-a84f-6e1a-e063-6294a90a2aae
Product NDC
87492-002
Form
LIQUID
Composition / generic term
Biotin
Labeler
Shenzhen yuehaotong Technology Co.,Ltd
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20260307 / 20310307

Source-listed ingredients

  • MINOXIDIL — 5 mg/100mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 5 mL in 1 BOX (87492-002-01) · 87492-002-01
  • 15 mL in 1 BOX (87492-002-02) · 87492-002-02
  • 30 mL in 1 BOX (87492-002-03) · 87492-002-03
  • 50 mL in 1 BOX (87492-002-04) · 87492-002-04
  • 100 mL in 1 BOX (87492-002-05) · 87492-002-05

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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