NDC 72187-0102-03 - ORSERDU

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: 72187-0102
Requested NDC: 72187-0102-03
Package NDCs from labels: 72187-0102-3, 72187-0102-03
Manufacturer: Stemline Therapeutics, Inc.
Effective date: 2026-06-24
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
ORSERDU - Stemline Therapeutics, Inc.	Stemline Therapeutics, Inc.	2026-06-24	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72187-0102-3	ORSERDU	30 in 1 BOTTLE	TABLET, FILM COATED	30		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72187-0102	ORSERDU (ELACESTRANT) TABLET, FILM COATED [STEMLINE THERAPEUTICS, INC.]	5	Current NDC, 1 package rows	20240805_aa66ae5c-2bd2-4444-8178-b55651e054ef.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
72187-0102-3	EA - Each	72187-0102	bd3f453f-0856-4231-b99c-e89eb7601751	1	2023-03-13

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ORSERDU	ELACESTRANT	Stemline Therapeutics, Inc.	aa66ae5c-2bd2-4444-8178-b55651e054ef	2026-06-24	Warnings, Adverse reactions	Exact identifier application number: NDA217639 ndc (package): 72187-0102-3 ndc (package): 72187-0101-3 ndc (product): 72187-0101 ndc (product): 72187-0102 ndc11 (package): 72187010203 rxcui: 2628489 rxcui: 2628484 rxcui: 2628478 rxcui: 2628487 spl id: 040abaf0-7a15-11f1-b55a-0800200c9a66 spl set id: aa66ae5c-2bd2-4444-8178-b55651e054ef unii: FM6A2627A8

Reported adverse events (FAERS/openFDA)#

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