NDC 72572-520-01 - Ondansetron

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: 72572-520
Requested NDC: 72572-520-01
Package NDCs from labels: 72572-520-01, 72572-520-25
Manufacturer: Civica, Inc. | Hikma Pharmaceuticals USA Inc.
Effective date: 2026-04-19
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Ondansetron - Civica, Inc. \| Hikma Pharmaceuticals USA Inc.	Civica, Inc. \| Hikma Pharmaceuticals USA Inc.	2026-04-19	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72572-520-01	Ondansetron	2 mL in 1 VIAL	INJECTION	2		3
72572-520-25	Ondansetron	25 in 1 CARTON	INJECTION	25		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72572-520	ONDANSETRON INJECTION [CIVICA, INC.]	3	Current NDC, Legacy NDC, 2 package rows	20220525_70437694-0341-4f3b-824c-06843403443f.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
72572-520-01	ML - Milliliter	72572-520	3ca7493e-8827-46b3-83c5-7fcf2aabcad8	1	2019-12-10
72572-520-25	ML - Milliliter	72572-520	564337fc-db4d-4bc3-ae10-9b510ed38e93	1	2019-12-10

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 59 of 59 · 1,161 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Lactated Ringers	SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE	Baxter Healthcare Corporation	f09f80bf-2f8b-4420-865d-aec2d5e5cd4d	2012-06-12		Exact identifier unii: 451W47IQ8X

Reported adverse events (FAERS/openFDA)#

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