NDC 50844-197 - Aspirin

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: 50844-197
Package NDCs from labels: 50844-197-12
Manufacturer: L.N.K. International, Inc. | LNK International, Inc.
Effective date: 2019-08-14
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Quality Plus 44-157-NI-Delisted	L.N.K. International, Inc. \| LNK International, Inc.	2019-08-14	HUMAN OTC DRUG LABEL

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 42 of 42 · 824 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Aspirin	ASPIRIN	Richmond Pharmaceuticals, Inc.	6a4c897d-c2a8-41b8-98b7-e7da8e2819ec	2017-10-30	Warnings	Exact identifier unii: R16CO5Y76E
Aspirin	ASPIRIN	Advance Pharmaceutical Inc.	f2e7332a-bcd6-4aef-9e4c-a2cef5ea9464	2017-10-30	Warnings	Exact identifier unii: R16CO5Y76E
Aspirin	ASPIRIN	Advance Pharmaceutical Inc.	8977b821-2843-4436-bd3b-bb902a4b787e	2017-10-30	Warnings	Exact identifier unii: R16CO5Y76E
Aspirin	ASPIRIN	Advance Pharmaceutical Inc.	968afa79-eaae-4cd9-ba0d-3b5eaa466b58	2017-10-30	Warnings	Exact identifier unii: R16CO5Y76E

Reported adverse events (FAERS/openFDA)#

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