NDC 51079-890-17

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: 51079-890
Requested NDC: 51079-890-17
Package NDCs from labels: 51079-890-17
Manufacturer: National Council for Prescription Drug Programs
Effective date: 2012-07-24
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
National Council for Prescription Drug Programs indexing - billing unit	National Council for Prescription Drug Programs	2012-07-24	Indexing - Billing Unit

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
51079-890-01	EA - Each	51079-890	289ea5ea-671e-43eb-8649-09a8b3fe63a1	1	2012-07-24
51079-890-17	EA - Each	51079-890	96de277b-d557-4f88-b096-d1eaeb06c06d	1	2012-07-24
51079-890-19	EA - Each	51079-890	3ff5f851-3d43-4606-a446-664c6b4d8835	1	2012-07-24
51079-890-20	EA - Each	51079-890	c8e5c4d7-d7d9-4f03-a91f-52b9d5d10f62	1	2012-07-24

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 1 of 1 · 3 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
RIFAMPIN	RIFAMPIN	Coupler LLC	410a314f-83bf-d9b3-e063-6294a90a872c	2025-10-13	Warnings, Adverse reactions	Exact identifier application number: ANDA064150
RIFAMPIN	RIFAMPIN	PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS	28109dee-3e5e-492b-b7d9-9ba46c0b5324	2025-03-25	Warnings, Adverse reactions	Exact identifier application number: ANDA064150
RIFAMPIN	RIFAMPIN	EPIC PHARMA, LLC	0391f1e1-70d4-4b15-8b58-055bb6a385b8	2023-12-20	Warnings, Adverse reactions	Exact identifier application number: ANDA064150

Reported adverse events (FAERS/openFDA)#

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