NDC 70518-3064-01 - 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: 70518-3064
Requested NDC: 70518-3064-01
Package NDCs from labels: 70518-3064-0, 70518-3064-1, 70518-3064-01
Manufacturer: REMEDYREPACK INC.
Effective date: 2026-04-03
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 Rx only	REMEDYREPACK INC.	2026-04-03	HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
70518-3064-0	2023-03-15	Lovastatin Tablets, USP Rx only
70518-3064-1	2023-03-15	Lovastatin Tablets, USP Rx only
70518-3064-0	2023-01-30	Lovastatin Tablets, USP Rx only
70518-3064-1	2023-01-30	Lovastatin Tablets, USP Rx only

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70518-3064-0	Lovastatin	90 in 1 BOTTLE, PLASTIC	TABLET	90		6
70518-3064-1	Lovastatin	30 in 1 BLISTER PACK	TABLET	30		6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70518-3064	LOVASTATIN TABLET [REMEDYREPACK INC.]	4	Current NDC, Legacy NDC, 2 package rows	20240312_a902a95f-072a-4487-99a9-109a93f8b23c.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 · 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 rxcui: 197903 unii: 9LHU78OQFD
Lovastatin	LOVASTATIN	Teva Pharmaceuticals USA, Inc.	0e15feec-d27e-4861-8152-c5a8b8ccacd4	2020-08-01	Warnings, Adverse reactions	Exact identifier application number: ANDA075551 ndc (product): 0093-0928 rxcui: 197905 rxcui: 197904 rxcui: 197903 spl id: caf8172a-311b-447a-8c8b-e9d70c23c8e8 spl set id: 0e15feec-d27e-4861-8152-c5a8b8ccacd4 unii: 9LHU78OQFD
Lovastatin	LOVASTATIN	Proficient Rx LP	027bd594-6a0a-4e6d-bd3c-4f33fdb4166a	2020-04-01	Warnings, Adverse reactions	Exact identifier application number: ANDA075551 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.