NDC 42292-057-01 - Abiraterone Acetate

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 42292-057
Requested NDC: 42292-057-01
Package NDCs from labels: 42292-057-01, 42292-057-03
Manufacturer: Mylan Institutional Inc.
Effective date: 2021-12-21
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Abiraterone Acetate - Mylan Institutional Inc.	Mylan Institutional Inc.	2021-12-21	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
42292-057-01	EA - Each	42292-057	2a12e42d-f1c4-4353-8c69-bc76c56844e9	1	2020-07-13
42292-057-03	EA - Each	42292-057	544cba86-c958-4cac-b80d-1c9349f2bd3e	1	2020-07-13

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 3 of 3 · 41 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
d3aef164-ffc6-d7a6-e053-2a95a90a5711			caff75fb-9320-4f45-a3ac-d1755e679406	2021-12-21	Warnings, Adverse reactions	Exact identifier spl id: d3aef164-ffc6-d7a6-e053-2a95a90a5711 spl set id: caff75fb-9320-4f45-a3ac-d1755e679406

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.