Drugplain

Oleander 100 [hp_C]/1

Oleander · PELLET · Hahnemann Laboratories, INC.

No Recall History
Plain English

Oleander is a pellet containing oleander at 100 [hp_C]/1, taken oral. Manufactured by Hahnemann Laboratories, INC..

Key Facts

Brand Name
Oleander
Generic Name
Oleander
NDC Code (Product)
37662-1988
Manufacturer
Hahnemann Laboratories, INC.
Strength
100 [hp_C]/1
Dosage Form
PELLET
Route
ORAL
Marketing Status
Marketing Start
11/21/2022

Recall History

No Recall History

Side Effects Reported to FDA

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

anaemia2 reports
blood iron abnormal2 reports
c-reactive protein increased2 reports
febrile neutropenia2 reports
hepatic infection fungal2 reports
off label use2 reports
pyrexia2 reports
thrombocytopenia2 reports
tumour lysis syndrome2 reports
completed suicide1 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Relieves flatulence with incontinence * Uses: See symptoms on front panel.

Dosage & Administration

Adults and children: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.

Frequently Asked Questions

What is Oleander used for?

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

Is Oleander a controlled substance?

Oleander is not classified as a controlled substance by the DEA.

What is the generic name for Oleander?

The generic name for Oleander is Oleander. There are 1 other brand versions of Oleander.

What is the NDC code for Oleander 100 [hp_C]/1?

The NDC (National Drug Code) for Oleander 100 [hp_C]/1 is 37662-1988, listed by Hahnemann Laboratories, INC..

Product NDC

37662-1988

Package NDC

37662-1988-1

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

Data from openFDA · Public domain (CC0 1.0)