ABRILADA

Product NDC: 50090-7998
11-digit product format: 500907998
Labeler code: 50090
Product ID: 50090-7998_fa5fba33-fd55-4011-8871-2c2013b5a0e4
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: adalimumab-afzb
Dosage form: KIT
Labeler: A-S Medication Solutions
Application: BLA761118
Marketing category: BLA
Marketing start: 2023-12-14
Listing certified through: 2027-12-31
Current FDA listing: Yes

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.

Matched openFDA labels page 1 of 1 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ABRILADA	ADALIMUMAB-AFZB	A-S Medication Solutions	79943fe6-1249-4074-9aed-c53937820d0f	2026-06-18	Boxed warning, Warnings, Adverse reactions	Exact identifier application number: BLA761118 ndc (product): 50090-7998
ABRILADA	ADALIMUMAB-AFZB	Pfizer Laboratories Div Pfizer Inc	5ef1c7cf-466f-495e-8d13-82e2ddfa7a4f	2026-05-06	Boxed warning, Warnings, Adverse reactions	Exact identifier application number: BLA761118

Additional Listing Data#

Finished product: Yes
Brand name base: ABRILADA
Listing expiration: 2027-12-31

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
797544	Internal RxNorm lookup
2668064	Internal RxNorm lookup
2668071	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
79943fe6-1249-4074-9aed-c53937820d0f	Available on FDA.report

Purple Book Biologic Products#

BLA, Proprietary name, Proper name table
BLA	Proprietary name	Proper name	License type	Status	Latest source
761118	Abrilada	adalimumab-afzb	351(k) Interchangeable	Rx	2026-06-01

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Status
50090-7998-0	50090799800	2 KIT in 1 CARTON (50090-7998-0) / 1 KIT in 1 KIT * .8 mL in 1 SYRINGE (0025-0318-01) * 1 mL in 1 PACKET (0069-1111-01)	2 kit	2026-06-17	0	Current