NDC 68094-752-59

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: 68094-752
Requested NDC: 68094-752-59
Package NDCs from labels: 68094-752-59
Manufacturer: National Council for Prescription Drug Programs
Effective date: 2012-07-24
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
National Council for Prescription Drug Programs indexing - billing unit	National Council for Prescription Drug Programs	2012-07-24	Indexing - Billing Unit

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
68094-752-59	ML - Milliliter	68094-752	43e58b47-ee98-429b-862b-7ab30715d59c	1	2012-07-24
68094-752-62	ML - Milliliter	68094-752	9451db06-d8e2-43f8-bd15-11955801346e	1	2012-07-24

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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Digoxin	DIGOXIN	Atlantic Biologicals Corps	dcf907d9-0f0e-4ecc-a555-7e6dcc08c166	2025-12-11	Warnings, Adverse reactions	Exact identifier application number: NDA021648
Digoxin	DIGOXIN	Hikma Pharmaceuticals USA Inc.	1b7e5c6e-e052-41b0-a4ce-05dfe62faaaf	2025-04-10	Warnings, Adverse reactions	Exact identifier application number: NDA021648

Reported adverse events (FAERS/openFDA)#

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