NDC 70860-784-41 - Valproate Sodium

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: 70860-784
Requested NDC: 70860-784-41
Package NDCs from labels: 70860-784-41, 70860-784-05
Manufacturer: Athenex Pharmaceutical Division, LLC.
Effective date: 2025-01-28
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Valproate Sodium - Athenex Pharmaceutical Division, LLC.	Athenex Pharmaceutical Division, LLC.	2025-01-28	HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
70860-784-05	2024-03-05	C162847	48780-1	1030e365-44fe-111a-e063-dadaa90a10e2	These highlights do not include all the information needed to use VALPROATE SODIUM INJECTION safely and effectively. See full prescribing information for VALPROATE SODIUM INJECTION. VALPROATE SODIUM injection for intravenous injection Initial U.S. Approval: 1996
70860-784-05	2024-01-30	C162847	48780-1	1030e365-44fe-111a-e063-dadaa90a10e2	These highlights do not include all the information needed to use VALPROATE SODIUM INJECTION safely and effectively. See full prescribing information for VALPROATE SODIUM INJECTION. VALPROATE SODIUM injection for intravenous injection Initial U.S. Approval: 1996

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70860-784	VALPROATE SODIUM INJECTION, SOLUTION [ATHENEX PHARMACEUTICAL DIVISION, LLC.]	3	Legacy NDC	20250130_856ecdad-a8e0-4bda-a217-cd7948ddfa59.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
70860-784-05	ML - Milliliter	70860-784	241b5347-b23f-4cb5-abe6-6c4b06e9ab61	1	2023-04-07
70860-784-41	ML - Milliliter	70860-784	19ea9dc6-caba-405b-89d4-73725d4b774b	1	2023-06-06

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 11 of 11 · 202 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Eye Wash	WATER	CVS Pharmacy	049cee29-7ec2-4d5b-8308-f522acde43a7	2017-03-29	Warnings	Exact identifier unii: 059QF0KO0R
Sterile Water	WATER	Baxter Healthcare Company	210dc9ab-d6ca-4552-ac19-1be17792d290	2016-05-31	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

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