National Weed Mix
- Product NDC
- 22840-9351
- 11-digit product format
- 228409351
- Labeler code
- 22840
- Product ID
- 22840-9351_7b43b65a-bbff-133f-e053-2991aa0a3395
- Type
- NON-STANDARDIZED ALLERGENIC
- Nonproprietary name
- Xanthium strumarium, Ambrosia trifida, Chenopodium album, Amaranthus retroflexus and Ambrosia artemisiifolia
- Dosage form
- SOLUTION
- Route
- INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS
- Labeler
- Greer Laboratories, Inc.
- Application
- BLA101833
- Marketing category
- BLA
- Marketing start
- 1981-09-15
- Marketing end
- 0000-00-00
- Substance
- AMBROSIA ARTEMISIIFOLIA POLLEN; AMARANTHUS RETROFLEXUS POLLEN; CHENOPODIUM ALBUM POLLEN; XANTHIUM STRUMARIUM POLLEN; AMBROSIA TRIFIDA POLLEN
- Active strength
- 0 g/mL; g/mL; g/mL; g/mL; g/mL
- Pharmacologic classes
- Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS],Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Pollen [CS],Allergens [CS],Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS],Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS],Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Pollen [CS],Allergens [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record