short ragweed
Generic: ambrosia artemisiifolia
Labeler: allermed laboratories, inc.Drug Facts
Product Profile
Brand Name
short ragweed
Generic Name
ambrosia artemisiifolia
Labeler
allermed laboratories, inc.
Dosage Form
INJECTION
Routes
Active Ingredients
ambrosia artemisiifolia pollen 1 g/10mL
Manufacturer
Identifiers & Regulatory
Product NDC
49643-315
Product ID
49643-315_2beeb52f-4452-7e67-e063-6294a90a5477
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
BLA
Application Number
BLA103113
Listing Expiration
2026-12-31
Marketing Start
1982-03-22
Pharmacologic Class
Established (EPC)
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
49643315
Hyphenated Format
49643-315
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
short ragweed (source: ndc)
Generic Name
ambrosia artemisiifolia (source: ndc)
Application Number
BLA103113 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/10mL
Packaging
- 5 mL in 1 VIAL, MULTI-DOSE (49643-315-05)
- 10 mL in 1 VIAL, MULTI-DOSE (49643-315-10)
- 30 mL in 1 VIAL, MULTI-DOSE (49643-315-30)
- 50 mL in 1 VIAL, MULTI-DOSE (49643-315-50)
Packages (4)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["CUTANEOUS", "INTRADERMAL", "SUBCUTANEOUS"], "spl_id": "2beeb52f-4452-7e67-e063-6294a90a5477", "openfda": {"nui": ["N0000185006", "N0000175629", "N0000184306", "N0000185001", "M0017130", "M0000728"], "unii": ["K20Y81ACO3"], "rxcui": ["896140"], "spl_set_id": ["1482f8a2-c2c0-45a1-8e90-b427227f0b28"], "pharm_class_cs": ["Pollen [CS]", "Allergens [CS]"], "pharm_class_pe": ["Increased Histamine Release [PE]", "Cell-mediated Immunity [PE]", "Increased IgG Production [PE]"], "pharm_class_epc": ["Standardized Pollen Allergenic Extract [EPC]"], "manufacturer_name": ["Allermed Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 VIAL, MULTI-DOSE (49643-315-05)", "package_ndc": "49643-315-05", "marketing_start_date": "19820322"}, {"sample": false, "description": "10 mL in 1 VIAL, MULTI-DOSE (49643-315-10)", "package_ndc": "49643-315-10", "marketing_start_date": "19820322"}, {"sample": false, "description": "30 mL in 1 VIAL, MULTI-DOSE (49643-315-30)", "package_ndc": "49643-315-30", "marketing_start_date": "19820322"}, {"sample": false, "description": "50 mL in 1 VIAL, MULTI-DOSE (49643-315-50)", "package_ndc": "49643-315-50", "marketing_start_date": "19820322"}], "brand_name": "Short Ragweed", "product_id": "49643-315_2beeb52f-4452-7e67-e063-6294a90a5477", "dosage_form": "INJECTION", "pharm_class": ["Allergens [CS]", "Cell-mediated Immunity [PE]", "Increased Histamine Release [PE]", "Increased IgG Production [PE]", "Pollen [CS]", "Standardized Pollen Allergenic Extract [EPC]"], "product_ndc": "49643-315", "generic_name": "Ambrosia artemisiifolia", "labeler_name": "Allermed Laboratories, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Short Ragweed", "active_ingredients": [{"name": "AMBROSIA ARTEMISIIFOLIA POLLEN", "strength": "1 g/10mL"}], "application_number": "BLA103113", "marketing_category": "BLA", "marketing_start_date": "19820322", "listing_expiration_date": "20261231"}