NDC 70518-0876-00 - PRAVASTATIN SODIUM

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: 70518-0876
Requested NDC: 70518-0876-00
Package NDCs from labels: 70518-0876-0, 70518-0876-1, 70518-0876-2, 70518-0876-00
Manufacturer: REMEDYREPACK INC.
Effective date: 2026-08-21
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
PRAVASTATIN SODIUM - REMEDYREPACK INC.	REMEDYREPACK INC.	2026-08-21	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
70518-0876-0	PRAVASTATIN SODIUM	90 in 1 BOTTLE, PLASTIC	TABLET	90	20
70518-0876-1	PRAVASTATIN SODIUM	30 in 1 BLISTER PACK	TABLET	30	20
70518-0876-2	PRAVASTATIN SODIUM	45 in 1 BOTTLE, PLASTIC	TABLET	45	20

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70518-0876	PRAVASTATIN SODIUM TABLET [REMEDYREPACK INC.]	15	Current NDC, Legacy NDC, 3 package rows	20250503_5ecd9fd1-7662-412d-99c5-13c77188748c.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 7 of 7 · 122 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
PRAVASTATIN SODIUM	PRAVASTATIN SODIUM	Proficient Rx LP	63ca6179-6ae3-4f0b-bdca-50d200317921	2019-10-01	Warnings, Adverse reactions	Exact identifier rxcui: 904475 unii: 3M8608UQ61
Pravastatin sodium	PRAVASTATIN SODIUM	Dr.Reddy's Laboratories Limited	99cc0546-bb2d-751e-edfd-1c15a1182e0c	2018-11-21	Warnings, Adverse reactions	Exact identifier rxcui: 904458 rxcui: 904481 rxcui: 904467 rxcui: 904475 unii: 3M8608UQ61

Reported adverse events (FAERS/openFDA)#

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