United States · FDA National Drug Code directory

Bryonia

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
0220-0946_47a9e355-d7f5-1e8d-e063-6394a90aba8b
Product NDC
0220-0946
Form
PELLET
Composition / generic term
BRYONIA ALBA ROOT
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
19830303
Source listing expiry
20271231

Source-listed ingredients

  • BRYONIA ALBA ROOT — 1 [hp_M]/[hp_M]

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 [hp_M] in 1 TUBE (0220-0946-41) · 0220-0946-41

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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