NDC 70518-4276-01 - Lorazepam

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: 70518-4276
Requested NDC: 70518-4276-01
Package NDCs from labels: 70518-4276-1, 70518-4276-0, 70518-4276-3, 70518-4276-2, 70518-4276-01
Manufacturer: REMEDYREPACK INC.
Effective date: 2026-09-03
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Lorazepam Tablets, USP CIV	REMEDYREPACK INC.	2026-09-03	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
70518-4276-0	Lorazepam	100 in 1 BOX	TABLET	100	3
70518-4276-1	Lorazepam	1 in 1 POUCH	TABLET	1	3
70518-4276-2	Lorazepam	100 in 1 BOX	TABLET	100	3
70518-4276-3	Lorazepam	1 in 1 POUCH	TABLET	1	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70518-4276	LORAZEPAM TABLET [REMEDYREPACK INC.]	2	Current NDC, 4 package rows	20250418_86630bdd-13ad-4ab5-9e94-fcf2ea2113e1.zip

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 6 of 6 · 102 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Lorazepam	LORAZEPAM	Aphena Pharma Solutions - Tennessee, LLC	a4fa14be-cef1-4b4b-b099-abde92f15145	2019-01-08	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 197900 unii: O26FZP769L
Lorazepam	LORAZEPAM	Aphena Pharma Solutions - Tennessee, LLC	08bd30b0-a1c1-4ec3-bb9c-b1d55ac59f75	2018-11-05	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 197902 unii: O26FZP769L

Reported adverse events (FAERS/openFDA)#

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