Home NDC 69448-018 IMULDOSA
Product NDC 69448-018
11-digit product format 694480018
Labeler code 69448
Product ID 69448-018_450dafe8-f537-6303-e063-6394a90aa784
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name ustekinumab-srlf
Dosage form INJECTION
Route SUBCUTANEOUS
Labeler Accord BioPharma Inc.
Application BLA761364
Marketing category BLA
Marketing start 2024-10-14
Substance USTEKINUMAB-SRLF
Active strength 90 mg/mL
Pharmacologic classes Interleukin-12 Antagonist [EPC], Interleukin-12 Antagonists [MoA], Interleukin-23 Antagonist [EPC], Interleukin-23 Antagonists [MoA]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base IMULDOSA
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength USTEKINUMAB-SRLF 90 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination FU77B4U5Z0 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 6 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2717067 Internal RxNorm lookup 2717074 Internal RxNorm lookup 2717078 Internal RxNorm lookup 2717083 Internal RxNorm lookup 2717085 Internal RxNorm lookup 2717086 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69448-018-63 IMULDOSA 1 in 1 BLISTER PACK INJECTION 1 9 69448-018-63 IMULDOSA 1 in 1 CARTON INJECTION 1 9
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 761364 Imuldosa ustekinumab-srlf 351(k) Interchangeable Rx 2026-08-01
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 69448-018-63 69448001863 1 BLISTER PACK in 1 CARTON (69448-018-63) / 1 SYRINGE in 1 BLISTER PACK / 1 mL in 1 SYRINGE 1 blister pack 2024-10-14 No No Current