NDC 70518-4459-01 - Folic Acid

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: 70518-4459
Requested NDC: 70518-4459-01
Package NDCs from labels: 70518-4459-0, 70518-4459-1, 70518-4459-01
Manufacturer: REMEDYREPACK INC.
Effective date: 2026-09-11
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Folic Acid	REMEDYREPACK INC.	2026-09-11	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70518-4459-0	Folic Acid	30 in 1 BLISTER PACK	TABLET	30		2
70518-4459-1	Folic Acid	7 in 1 BLISTER PACK	TABLET	7		2

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 10 of 10 · 183 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Foltrexyl	FOLIC ACID, VITAMIN D3	PureTek Corporation	b2d71f92-018f-183e-e053-2995a90a5db0	2020-10-29	Warnings, Adverse reactions	Exact identifier unii: 935E97BOY8
FOLIC ACID	FOLIC ACID	Leading Pharma, LLC	1ba8c407-9613-4319-ac40-0a429cb0f3f4	2019-02-19	Warnings, Adverse reactions	Exact identifier rxcui: 310410 unii: 935E97BOY8
Folic Acid	FOLIC ACID	Aphena Pharma Solutions - Tennessee, LLC	d6c7ac9b-f44a-4f10-9d1d-efbebd37c313	2019-02-12	Warnings, Adverse reactions	Exact identifier rxcui: 310410 unii: 935E97BOY8

Reported adverse events (FAERS/openFDA)#

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