Drugplain

Plumeria Rubra 30 [hp_C]/1

Plumeria Rubra · PELLET · Hahnemann Laboratories, INC.

No Recall History
Plain English

Plumeria Rubra is a pellet containing plumeria rubra at 30 [hp_C]/1, taken oral. Manufactured by Hahnemann Laboratories, INC..

Key Facts

Brand Name
Plumeria Rubra
Generic Name
Plumeria Rubra
NDC Code (Product)
37662-3345
Manufacturer
Hahnemann Laboratories, INC.
Strength
30 [hp_C]/1
Dosage Form
PELLET
Route
ORAL
Marketing Status
Marketing Start
06/13/2023

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

arthralgia1 reports
asthenia1 reports
drug ineffective1 reports
fatigue1 reports
fibromyalgia1 reports
gait disturbance1 reports
gait inability1 reports
hypertension1 reports
miliaria1 reports
muscle mass1 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Frequently Asked Questions

What is Plumeria Rubra used for?

Plumeria Rubra contains Plumeria Rubra. It is a pellet taken oral. Consult your doctor for specific uses.

Is Plumeria Rubra a controlled substance?

Plumeria Rubra is not classified as a controlled substance by the DEA.

What is the generic name for Plumeria Rubra?

The generic name for Plumeria Rubra is Plumeria Rubra. There are no other listed brand versions of Plumeria Rubra.

What is the NDC code for Plumeria Rubra 30 [hp_C]/1?

The NDC (National Drug Code) for Plumeria Rubra 30 [hp_C]/1 is 37662-3345, listed by Hahnemann Laboratories, INC..

Product NDC

37662-3345

Package NDC

37662-3345-1

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)