Medusa 500 [hp_C]/1
Medusa · PELLET · Hahnemann Laboratories, INC.
Medusa is an over-the-counter oral pellet medication available in a 500-unit strength. Please consult the product packaging or a healthcare provider for information about its specific uses and intended purpose.
Key Facts
- Brand Name
- Medusa
- Generic Name
- Medusa
- NDC Code (Product)
37662-1807- Manufacturer
- Hahnemann Laboratories, INC.
- Strength
- 500 [hp_C]/1
- Dosage Form
- PELLET
- Route
- ORAL
- Marketing Status
- Marketing Start
- 10/31/2022
Recall History
No Recall HistoryFull Prescribing Information
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 500-unit strength. Please consult the product packaging or a healthcare provider for information about its specific uses and intended purpose.
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 500 [hp_C]/1?
The NDC (National Drug Code) for Medusa 500 [hp_C]/1 is 37662-1807, listed by Hahnemann Laboratories, INC..
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)