Drugplain

Medusa 100 [hp_C]/1

Medusa · PELLET · Hahnemann Laboratories, INC.

No Recall History
Plain English

Medusa is an over-the-counter oral pellet medication available in a 100 unit strength. The specific condition it treats and its drug class information are not provided in the available data.

Key Facts

Brand Name
Medusa
Generic Name
Medusa
NDC Code (Product)
37662-1805
Manufacturer
Hahnemann Laboratories, INC.
Strength
100 [hp_C]/1
Dosage Form
PELLET
Route
ORAL
Marketing Status
Marketing Start
10/31/2022

Recall History

No Recall History

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Hives on the face*

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 Medusa used for?

Medusa is an over-the-counter oral pellet medication available in a 100 unit strength. The specific condition it treats and its drug class information are not provided in the available data.

Is Medusa a controlled substance?

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

What is the generic name for Medusa?

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

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

The NDC (National Drug Code) for Medusa 100 [hp_C]/1 is 37662-1805, listed by Hahnemann Laboratories, INC..

Product NDC

37662-1805

Package NDC

37662-1805-1

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

Data from openFDA · Public domain (CC0 1.0)