United States · FDA National Drug Code directory

Berberis aquifolium

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
0220-0831_3bf0f995-f31f-0716-e063-6294a90a1552
Product NDC
0220-0831
Form
PELLET
Composition / generic term
BERBERIS AQUIFOLIUM ROOT BARK
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
19830303
Source listing expiry
20261231

Source-listed ingredients

  • BERBERIS AQUIFOLIUM ROOT BARK — 30 [hp_C]/30[hp_C]

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 [hp_C] in 1 TUBE (0220-0831-41) · 0220-0831-41

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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Berberis aquifolium — United States | Molindra Medicines