Rhus Glabra 200 [hp_C]/1
Rhus Glabra · PELLET · Hahnemann Laboratories, INC.
No Recall History
Plain English
Rhus Glabra is a pellet containing rhus glabra at 200 [hp_C]/1, taken oral. Manufactured by Hahnemann Laboratories, INC..
Key Facts
- Brand Name
- Rhus Glabra
- Generic Name
- Rhus Glabra
- NDC Code (Product)
37662-1376- Manufacturer
- Hahnemann Laboratories, INC.
- Strength
- 200 [hp_C]/1
- Dosage Form
- PELLET
- Route
- ORAL
- Marketing Status
- Marketing Start
- 08/18/2022
Recall History
No Recall HistoryFull Prescribing Information
Source: FDA Drug Label (SPL)For healthcare professionals
Frequently Asked Questions
What is Rhus Glabra used for?
Rhus Glabra contains Rhus Glabra. It is a pellet taken oral. Consult your doctor for specific uses.
Is Rhus Glabra a controlled substance?
Rhus Glabra is not classified as a controlled substance by the DEA.
What is the generic name for Rhus Glabra?
The generic name for Rhus Glabra is Rhus Glabra. There are no other listed brand versions of Rhus Glabra.
What is the NDC code for Rhus Glabra 200 [hp_C]/1?
The NDC (National Drug Code) for Rhus Glabra 200 [hp_C]/1 is 37662-1376, 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)