NDC 70518-2195-01 - Torsemide

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: 70518-2195
Requested NDC: 70518-2195-01
Package NDCs from labels: 70518-2195-0, 70518-2195-1, 70518-2195-01
Manufacturer: REMEDYREPACK INC.
Effective date: 2026-07-21
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Torsemide - REMEDYREPACK INC.	REMEDYREPACK INC.	2026-07-21	HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2023-03-08	These highlights do not include all the information needed to use TORSEMIDE TABLETS safely and effectively. See full prescribing information for TORSEMIDE TABLETS. TORSEMIDE tablets, for oral use Initial U.S. Approval: 1993
2023-03-08	These highlights do not include all the information needed to use TORSEMIDE TABLETS safely and effectively. See full prescribing information for TORSEMIDE TABLETS. TORSEMIDE tablets, for oral use Initial U.S. Approval: 1993
2023-01-30	These highlights do not include all the information needed to use TORSEMIDE TABLETS safely and effectively. See full prescribing information for TORSEMIDE TABLETS. TORSEMIDE tablets, for oral use Initial U.S. Approval: 1993
2023-01-30	These highlights do not include all the information needed to use TORSEMIDE TABLETS safely and effectively. See full prescribing information for TORSEMIDE TABLETS. TORSEMIDE tablets, for oral use Initial U.S. Approval: 1993

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70518-2195-0	Torsemide	90 in 1 BOTTLE, PLASTIC	TABLET	90		6
70518-2195-1	Torsemide	90 in 1 BOTTLE, PLASTIC	TABLET	90		6

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 5 of 5 · 94 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Equaline Advanced Relief Eye Drops	DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HYDROCHLORIDE	United Natural Foods, Inc.	f7602789-179a-edfc-e053-6294a90a0844	2023-12-20	Warnings	Exact identifier unii: FZ989GH94E
Topcare Health Artificial Tears	POLYVINYL ALCOHOL, POVIDONE	Topco Associates LLC	9c614c0e-5862-682f-e053-2a95a90abc09	2023-12-20	Warnings	Exact identifier unii: FZ989GH94E
TopCare Health Advanced Moisturizing Plus Redness Relief	DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCL	Topco Associates LLC	9c6193a6-d822-1b27-e053-2995a90ab3cf	2023-12-20	Warnings	Exact identifier unii: FZ989GH94E
HEB Advanced Eye Drops	DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HYDROCHLORIDE	HEB Grocery Company, LP	f76281d6-3aea-349b-e053-6394a90afca2	2023-12-20	Warnings	Exact identifier unii: FZ989GH94E
Good Neighbor Pharmacy Artifical Tears Lubricant Eye Drops	POLYVINYL ALCOHOL, POVIDONE	Proficient Rx LP	73e12596-6dd5-4cd2-83ed-992e1211b4b8	2023-12-01	Warnings	Exact identifier unii: FZ989GH94E
Torsemide	TORSEMIDE	Hikma Pharmaceuticals USA Inc.	fde1d1be-0faa-440a-9039-bdb103288c76	2023-08-31	Warnings, Adverse reactions	Exact identifier application number: ANDA076943 ndc (product): 0054-0077 rxcui: 198371 spl id: 978f435d-eae6-49b7-80cd-6c951abce99f spl set id: fde1d1be-0faa-440a-9039-bdb103288c76 unii: W31X2H97FB
Torsemide	TORSEMIDE	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	03fbbb85-4e0f-4f3b-b4b0-87f84cb33d47	2023-06-30	Warnings, Adverse reactions	Exact identifier rxcui: 198371 unii: W31X2H97FB
Torsemide	TORSEMIDE	A-S Medication Solutions	3e9c6ee1-c49f-4f59-9391-8a9b57becb02	2023-05-25	Warnings, Adverse reactions	Exact identifier unii: W31X2H97FB
Torsemide	TORSEMIDE	A-S Medication Solutions	3ed913ba-f0c0-4ba5-9440-73c4374f4226	2023-05-25	Warnings, Adverse reactions	Exact identifier rxcui: 198371 unii: W31X2H97FB
Torsemide	TORSEMIDE	Bryant Ranch Prepack	f24151c8-02cd-4b07-a7fd-796903210aba	2023-05-23	Warnings, Adverse reactions	Exact identifier unii: W31X2H97FB
Torsemide	TORSEMIDE	NCS HealthCare of KY, LLC dba Vangard Labs	201e892d-d963-4c6a-b35b-c5780b01f659	2022-12-15	Warnings, Adverse reactions	Exact identifier rxcui: 198371 unii: W31X2H97FB
Torsemide	TORSEMIDE	Aphena Pharma Solutions - Tennessee, LLC	b869bc45-1ebb-42fb-82c5-603f09835790	2017-10-19	Warnings, Adverse reactions	Exact identifier application number: ANDA076943 rxcui: 198371 unii: W31X2H97FB
Torsemide	TORSEMIDE	Camber Pharmaceuticals, Inc.	0d4a4ef9-0944-452c-b014-bd822bfb9dd9	2017-08-14	Warnings, Adverse reactions	Exact identifier rxcui: 198371 unii: W31X2H97FB
Torsemide	TORSEMIDE	Teva Pharmaceuticals USA, Inc.	8a95cbdb-0601-47a5-9b3a-0c3b0629ceb9	2017-02-28	Warnings, Adverse reactions	Exact identifier rxcui: 198371 unii: W31X2H97FB

Reported adverse events (FAERS/openFDA)#

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