NDC 70518-2425-01 - Lovastatin

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: 70518-2425
Requested NDC: 70518-2425-01
Package NDCs from labels: 70518-2425-0, 70518-2425-1, 70518-2425-01
Manufacturer: REMEDYREPACK INC.
Effective date: 2026-07-23
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Lovastatin Tablet USP	REMEDYREPACK INC.	2026-07-23	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70518-2425-0	Lovastatin	30 in 1 BLISTER PACK	TABLET	30		4
70518-2425-1	Lovastatin	90 in 1 BOTTLE, PLASTIC	TABLET	90		4

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 4 of 4 · 64 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Lovastatin	LOVASTATIN	Proficient Rx LP	c2b1b926-def3-4411-9aed-395b969028fe	2021-01-01	Warnings, Adverse reactions	Exact identifier application number: ANDA075991 rxcui: 197903 unii: 9LHU78OQFD
Lovastatin	LOVASTATIN	Teva Pharmaceuticals USA, Inc.	0e15feec-d27e-4861-8152-c5a8b8ccacd4	2020-08-01	Warnings, Adverse reactions	Exact identifier rxcui: 197905 rxcui: 197904 rxcui: 197903 unii: 9LHU78OQFD
Lovastatin	LOVASTATIN	Proficient Rx LP	027bd594-6a0a-4e6d-bd3c-4f33fdb4166a	2020-04-01	Warnings, Adverse reactions	Exact identifier rxcui: 197904 unii: 9LHU78OQFD
Lovastatin	LOVASTATIN	Proficient Rx LP	f9e27117-db98-48bc-b7bc-fc98c9b719cf	2019-11-01	Warnings, Adverse reactions	Exact identifier rxcui: 197903 unii: 9LHU78OQFD

Reported adverse events (FAERS/openFDA)#

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