United States · FDA National Drug Code directory
Plumeria Rubra
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
- 37662-3350_fe101e58-b959-14ec-e053-6294a90a6118
- Product NDC
- 37662-3350
- Form
- PELLET
- Composition / generic term
- Plumeria Rubra
- Labeler
- Hahnemann Laboratories, INC.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 20230613
- Source listing expiry
- 20261231
Source-listed ingredients
- PLUMERIA RUBRA WHOLE — 10 [hp_M]/1
These values do not establish equivalence or a dose recommendation.
Packages
- 200 PELLET in 1 VIAL, GLASS (37662-3350-1) · 37662-3350-1
- 500 PELLET in 1 VIAL, GLASS (37662-3350-2) · 37662-3350-2
- 3000 PELLET in 1 BOTTLE, GLASS (37662-3350-3) · 37662-3350-3
- 10000 PELLET in 1 BOTTLE, GLASS (37662-3350-4) · 37662-3350-4
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.
Browse United States records →