short ragweed

Generic: ambrosia artemisiifolia

Labeler: allermed laboratories, inc.
NDC Directory HUMAN PRESCRIPTION DRUG BLA Inactive Finished

Drug Facts

Product Profile

Brand Name short ragweed
Generic Name ambrosia artemisiifolia
Labeler allermed laboratories, inc.
Dosage Form INJECTION
Routes
CUTANEOUS INTRADERMAL SUBCUTANEOUS
Active Ingredients

ambrosia artemisiifolia pollen 1 g/10mL

Manufacturer
Allermed Laboratories, Inc.

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)
standardized pollen allergenic extract [epc]
Chemical Structure
pollen [cs] allergens [cs]
Physiologic Effect
increased histamine release [pe] cell-mediated immunity [pe] increased igg production [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 49643315
Hyphenated Format 49643-315

Supplemental Identifiers

RxCUI
896140
UNII
K20Y81ACO3
NUI
N0000185006 N0000175629 N0000184306 N0000185001 M0017130 M0000728

Packaging Origin

Original Packager
true

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
CUTANEOUS INTRADERMAL SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 1 g/10mL
source: ndc
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)
source: ndc

Packages (4)

Ingredients (1)

ambrosia artemisiifolia pollen (1 g/10mL)

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"}