NDC 71872-7352-01 - Heparin 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
71872-7352
Requested NDC
71872-7352-01
Package NDCs from labels
71872-7352-1, 71872-7352-01
Manufacturer
Medical Purchasing Solutions, LLC
Effective date
2025-09-15
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Heparin Sodium - Medical Purchasing Solutions, LLCMedical Purchasing Solutions, LLC2025-09-15HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71872-7352-1Heparin Sodium1 in 1 BAGINJECTION11
71872-7352-1Heparin Sodium30 mL in 1 VIAL, MULTI-DOSEINJECTION301

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 21 · 414 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
NitrogenNITROGENMinneapolis Oxygen Companyc3fdbc5c-da70-4cbd-bdee-eddb4d852b262025-12-01Exact identifier
unii: N762921K75
Heparin SodiumHEPARIN SODIUMFresenius Kabi USA, LLCd55b4a63-0c04-4874-b74f-9e9b9e8b008c2025-11-28Warnings, Adverse reactionsExact identifier
rxcui: 1361226
rxcui: 1361615
unii: ZZ45AB24CA
Heparin SodiumHEPARIN SODIUMFresenius Kabi USA, LLCed937dd2-8fab-4875-a1e8-627b71ccb7fb2025-11-27Warnings, Adverse reactionsExact identifier
rxcui: 1361226
rxcui: 1361615
unii: ZZ45AB24CA
Thermacare Heat Therapy Max Strength Lidocaine Pain Relief RollonTHERMACARE HEAT THERAPY MAX STRENGTH LIDOCAINE PAIN RELIEF ROLLONClarion Brands LLC4482d34d-eaca-5522-e063-6394a90a6afb2025-11-26WarningsExact identifier
unii: LKG8494WBH
NITROGENNITROGENLampton Welding Supply Company, Inc125eedfb-8ab0-42b3-8393-7e8b9313020b2025-11-26Exact identifier
unii: N762921K75
NITROGENNITROGENVolunteer Welding Supply Incc4c1b8a0-d957-44f8-a7d1-aefe9b251b662025-11-26Exact identifier
unii: N762921K75
NitrogenNITROGENSuper Gas, Inc.80a178d8-7173-4e7a-ace9-7fe3fd0e07242025-11-26Exact identifier
unii: N762921K75
NitrogenNITROGENGeneral Air Service & Supply Co8e44ea92-d052-438a-b850-ccd147906e472025-11-26Exact identifier
unii: N762921K75
NitrogenNITROGENWestair Gases & Equipment, Inc.0268620b-4e8b-4b62-a768-688b477e01712025-11-26Exact identifier
unii: N762921K75
NitrogenNITROGENYoung Welding Supply, Inc86565775-ba7a-4e84-a9d9-72806a871b592025-11-26Exact identifier
unii: N762921K75
NitrogenNITROGENDale Oxygen And Acetylene Service, Incb4d03108-9837-495b-bf0d-2bb929cb7e392025-11-25Exact identifier
unii: N762921K75
NitrogenNITROGENMississippi Welders Supply Company, Inc.02b3fd81-4792-4dd6-9efb-1c3d58132a882025-11-25Exact identifier
unii: N762921K75
NITROGENNITROGENMedical-Technical Gases, Inc.eb3cfc21-907d-ae13-e053-2a95a90a15c62025-11-25Exact identifier
unii: N762921K75
NitrogenNITROGENOxarc, LLC74d62331-0e9e-4983-90e9-4de506fcfdcf2025-11-25Exact identifier
unii: N762921K75
NitrogenNITROGENS. J. Smith Co., Inc.d85670e1-a5e8-466d-bf58-9d6c75b2a6912025-11-25Exact identifier
unii: N762921K75
PUR-WASHWATERNiagara Pharmaceuticals Inc.beda35c3-9a8b-47ad-e053-2995a90a7b1b2025-11-24WarningsExact identifier
unii: 059QF0KO0R
Easy Care First Aid EyewashWATERTender Corporationa070aac8-e6d2-ef10-e053-2a95a90aa5b12025-11-24WarningsExact identifier
unii: 059QF0KO0R
PUR-WASHWATERNiagara Pharmaceuticals Inc.e07a064b-f680-405c-bbcd-24fac430951e2025-11-24WarningsExact identifier
unii: 059QF0KO0R
ULINE EyewashEYEWASHNiagara Pharmaceuticals Inc.2d7f22d2-320b-6af1-e063-6294a90addc62025-11-24WarningsExact identifier
unii: 059QF0KO0R
Pur-WashEYEWASHNiagara Pharmaceuticals, Inc.0d43b1c1-2699-37f1-e054-00144ff88e882025-11-24WarningsExact identifier
unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

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