NDC 70518-2009-01 - 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: 70518-2009
Requested NDC: 70518-2009-01
Package NDCs from labels: 70518-2009-0, 70518-2009-1, 70518-2009-01
Manufacturer: REMEDYREPACK INC.
Effective date: 2026-05-21
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
LOVASTATIN TABLETS USP 10 mg, 20 mg and 40 mg Rx only	REMEDYREPACK INC.	2026-05-21	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70518-2009-0	Lovastatin	90 in 1 BOTTLE, PLASTIC	TABLET	90		13
70518-2009-1	Lovastatin	30 in 1 BLISTER PACK	TABLET	30		13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70518-2009	LOVASTATIN TABLET [REMEDYREPACK INC.]	9	Current NDC, Legacy NDC, 2 package rows	20240120_ff040b3c-6790-40d7-bd64-a4073b4a2045.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 4 of 4 · 61 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Lovastatin	LOVASTATIN	Proficient Rx LP	f9e27117-db98-48bc-b7bc-fc98c9b719cf	2019-11-01	Warnings, Adverse reactions	Exact identifier application number: ANDA078296 rxcui: 197903 unii: 9LHU78OQFD

Reported adverse events (FAERS/openFDA)#

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