Ambrosia artemisiaefolia
- Product NDC
- 0220-0225
- 11-digit product format
- 002200225
- Labeler code
- 0220
- Product ID
- 0220-0225_947db1ea-d502-4d61-e053-2a95a90a0d96
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- AMBROSIA ARTEMISIIFOLIA
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1983-03-03
- Marketing end
- 2019-12-31
- Substance
- AMBROSIA ARTEMISIIFOLIA
- Active strength
- 6 [hp_X]/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record