Home NDC 49643-315-05 Short Ragweed
Product NDC 49643-315
Requested package NDC 49643-315-05
11-digit product format 496430315
Labeler code 49643
Product ID 49643-315_2beeb52f-4452-7e67-e063-6294a90a5477
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Ambrosia artemisiifolia
Dosage form INJECTION
Route CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Labeler Allermed Laboratories, Inc.
Application BLA103113
Marketing category BLA
Marketing start 1982-03-22
Substance AMBROSIA ARTEMISIIFOLIA POLLEN
Active strength 1 g/10mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Pollen [CS], Standardized Pollen Allergenic Extract [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…
Additional Listing Data#
Finished product Yes
Brand name base Short Ragweed
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AMBROSIA ARTEMISIIFOLIA POLLEN 1 g/10mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination K20Y81ACO3 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 896140 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 49643-315-05 Short Ragweed 5 mL in 1 VIAL, MULTI-DOSE INJECTION 5 6 49643-315-10 Short Ragweed 10 mL in 1 VIAL, MULTI-DOSE INJECTION 10 6 49643-315-30 Short Ragweed 30 mL in 1 VIAL, MULTI-DOSE INJECTION 30 6 49643-315-50 Short Ragweed 50 mL in 1 VIAL, MULTI-DOSE INJECTION 50 6
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49643-315 SHORT RAGWEED (AMBROSIA ARTEMISIIFOLIA) INJECTION [ALLERMED LABORATORIES, INC.] 5 Current NDC, Legacy NDC, 4 package rows 20240913_1482f8a2-c2c0-45a1-8e90-b427227f0b28.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Purple Book Biologic Products# BLA, Proprietary name, Proper name table BLA Proprietary name Proper name License type Status Latest source 103113 Pollens - Weeds and Garden Plants, Ragweed, Short Ambrosia artemisiifolia 351(a) Rx 2026-07-01
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 49643-315-05 49643031505 5 mL in 1 VIAL, MULTI-DOSE (49643-315-05) 5 ml 1982-03-22 0000-00-00 No No Current