Drugplain

Ambrosia artemisiaefolia 30 [hp_C]/30[hp_C]

AMBROSIA ARTEMISIIFOLIA · PELLET · Boiron

No Recall History
Plain English

Ambrosia artemisiaefolia is a pellet containing ambrosia artemisiifolia at 30 [hp_C]/30[hp_C], taken oral. Manufactured by Boiron.

Key Facts

Brand Name
Ambrosia artemisiaefolia
Generic Name
AMBROSIA ARTEMISIIFOLIA
NDC Code (Product)
0220-0219
Manufacturer
Boiron
Strength
30 [hp_C]/30[hp_C]
Dosage Form
PELLET
Route
ORAL
Marketing Status
Marketing Start
03/03/1983

Recall History

No Recall History

Side Effects Reported to FDA

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

abdominal pain1 reports
acne1 reports
adverse drug reaction1 reports
anxiety1 reports
blood disorder1 reports
deep vein thrombosis1 reports
dyspepsia1 reports
ear disorder1 reports
ecchymosis1 reports
epigastric discomfort1 reports

Frequently Asked Questions

What is Ambrosia artemisiaefolia used for?

Ambrosia artemisiaefolia contains AMBROSIA ARTEMISIIFOLIA. It is a pellet taken oral. Consult your doctor for specific uses.

Is Ambrosia artemisiaefolia a controlled substance?

Ambrosia artemisiaefolia is not classified as a controlled substance by the DEA.

What is the generic name for Ambrosia artemisiaefolia?

The generic name for Ambrosia artemisiaefolia is AMBROSIA ARTEMISIIFOLIA. There are 10 other brand versions of AMBROSIA ARTEMISIIFOLIA.

What is the NDC code for Ambrosia artemisiaefolia 30 [hp_C]/30[hp_C]?

The NDC (National Drug Code) for Ambrosia artemisiaefolia 30 [hp_C]/30[hp_C] is 0220-0219, listed by Boiron.