NDC 13985-805 - CMPK

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
13985-805
Package NDCs from labels
13985-805-50
Manufacturer
MWI (VetOne)
Effective date
2026-03-20
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
CMPK - MWI (VetOne)MWI (VetOne)2026-03-20PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
13985-805-50CMPK500 mL in 1 BOTTLE, PLASTICINJECTION, SOLUTION5004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
13985-805CMPK INJECTION, SOLUTION [MWI (VETONE)]31 package rows20151217_f2b27f49-9707-480c-90d8-430a09ef6c03.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Calcium Gluconate MonohydrateACTIVE INGREDIENTCZN0MI5R31CMPK INJECTION, SOLUTION [MWI (VETONE)]2
Dextrose MonohydrateACTIVE INGREDIENTLX22YL083GCMPK INJECTION, SOLUTION [MWI (VETONE)]2
Magnesium GluconateACTIVE INGREDIENTT42NAD2KHCCMPK INJECTION, SOLUTION [MWI (VETONE)]2
Potassium ChlorideACTIVE INGREDIENT660YQ98I10CMPK INJECTION, SOLUTION [MWI (VETONE)]2
Sodium Hypophosphite MonohydrateACTIVE INGREDIENT4VN69WUP7NCMPK INJECTION, SOLUTION [MWI (VETONE)]2
Calcium CationACTIVE MOIETY2M83C4R6ZBCMPK INJECTION, SOLUTION [MWI (VETONE)]2
DextroseACTIVE MOIETYIY9XDZ35W2CMPK INJECTION, SOLUTION [MWI (VETONE)]2
Magnesium cationACTIVE MOIETYT6V3LHY838CMPK INJECTION, SOLUTION [MWI (VETONE)]2
PhosphorusACTIVE MOIETY27YLU75U4WCMPK INJECTION, SOLUTION [MWI (VETONE)]2
Potassium cationACTIVE MOIETY295O53K152CMPK INJECTION, SOLUTION [MWI (VETONE)]2

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 27 of 31 · 616 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
DextroseDEXTROSE MONOHYDRATEBaxter Healthcare Company9c80dfee-8923-4d1f-85b0-98bd68b942122022-12-07Warnings, Adverse reactionsExact identifier
unii: LX22YL083G
DextroseDEXTROSE MONOHYDRATEBaxter Healthcare Corporation50603082-bce5-49eb-9737-e04239cfb6952022-12-07Warnings, Adverse reactionsExact identifier
unii: LX22YL083G
Multiple Electrolytes pH 7.4SODIUM CHLORIDE, SODIUM GLUCONATE, SODIUM ACETATE, POTASSIUM CHLORIDE AND MAGNESIUM CHLORIDEFresenius Kabi USA, LLC84221110-b3f1-42f4-800c-ad1d3b330e9e2022-11-10Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Multiple Electrolytes pH 5.5SODIUM CHLORIDE, SODIUM GLUCONATE, SODIUM ACETATE, POTASSIUM CHLORIDE AND MAGNESIUM CHLORIDEFresenius Kabi USA, LLCcf1f5f15-d31d-4a02-8f7e-b289d5ad4b5c2022-11-10Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Anticoagulant Citrate Phosphate Dextrose (CPD) Blood-Pack Units in PL 146 PlasticANTICOAGULANT CITRATE PHOSPHATE DEXTROSE (CPD) SOLUTIONFenwal, Inc.d55cb701-9664-4931-8754-1a8cae68da062022-11-01Exact identifier
unii: LX22YL083G
CPDA-1ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINE (CPDA-1) SOLUTIONFenwal, Inc.f9d7f1b4-7a77-44f9-8924-10b16008b49d2022-11-01Exact identifier
unii: LX22YL083G
Anticoagulant Citrate Phosphate Dextrose (CPD) Blood-Pack Units in PL 146 PlasticANTICOAGULANT CITRATE PHOSPHATE DEXTROSE (CPD)Fenwal, Inc.4a08a9ec-46a5-4fcf-80ee-5c33f1a8b7462022-11-01Exact identifier
unii: LX22YL083G
Potassium ChloridePOTASSIUM CHLORIDEZydus Pharmaceuticals (USA) Inc.31e02249-7984-4b8f-9e37-2b79b708ac082022-10-18Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Potassium ChloridePOTASSIUM CHLORIDEZydus Lifesciences Limited099c3a36-f460-4191-80e5-0c4153a5c7132022-10-18Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Potassium ChloridePOTASSIUM CHLORIDEBluePoint Laboratories73c911bb-4d39-4793-acba-90ed4b0eff462022-10-17Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
DextroseDEXTROSE MONOHYDRATEMedical Purchasing Solutions, LLC66713d9c-f404-4ec8-e053-2a91aa0a620a2022-10-13Warnings, Adverse reactionsExact identifier
unii: LX22YL083G
DextroseDEXTROSE MONOHYDRATEMedical Purchasing Solutions, LLC677bb6d6-704b-5be5-e053-2991aa0a5f6f2022-10-13Warnings, Adverse reactionsExact identifier
unii: LX22YL083G
Dextrose MonohydrateDEXTROSE MONOHYDRATEMedical Purchasing Solutions, LLCdc6664a6-1be1-676c-e053-2995a90a34902022-10-07Warnings, Adverse reactionsExact identifier
unii: LX22YL083G
Dr Talbots Infgant Gas Colic ReliefCARBO VEGETABILIS 12X,CHAMOMILLA 12X,FOENICULUM VULGARE 12X,LYCOPODIUM 30X,NUX MOSCHATA 12X,RAPHANUS SATIVUS 12X,ZINGIBER OFFICINALE 12X,KALI MURIATICUM 6X,MAGNESIA PHOSPHORICA 12X,NATRUM PHOSPHORICUM 6XTalbot's Pharmaceuticals Family Products,LLC.e8bee190-04b2-4be6-e053-2a95a90a30a02022-09-28WarningsExact identifier
unii: 660YQ98I10
Dr Talbots Infant Tummy Ache ReliefCALENDULA OFFICINALIS 12X,CARBO VEGETABILIS 12X,LYCOPODIUM 30X,FOENICULUM VULGARE 12X,NUX MOSCHATA 12X,ZINGIBER OFFICINALE 12X,KALI MURIATICUM 6X,MAGNESIA PHOSPHORICA 12X,NATRUM PHOSPHORICUM 6XTalbot's Pharmaceuticals Family Products,LLC.e9c24994-b935-36e6-e053-2a95a90a78df2022-09-28WarningsExact identifier
unii: 660YQ98I10
Dr Talbots Infant Mucus Cold ReliefEUPATORIUM PERF 12X,HEPAR SULPHURIS CALCAREUM 12X,KALI BICHROMICUM 12X,MARRUBIUM VULGARE 12X,PHOSPHORUS 30X,PULSATILLA 12X,RUMEX CRISPUS 12X,SAMBUCUS NIGRA 12X,CALCAREA SULPHURICA 12X,FERRUM PHOSPHORICUM 12XTalbots Pharmaceuticals Family Products, LLC.e8917c54-f4c2-3427-e053-2995a90adbf22022-09-13WarningsExact identifier
unii: 660YQ98I10
Dr Talbots Infant Pain Inflamtion ReliefARNICA 12X,BELLIS PERENNIS 12X,CALENDULA OFFICINALIS 12X,CHAMOMILLA 12X,COFFEA CRUDA 12X,HYPERICUM 12X,MILLEFOLIUM 12X,FERRUM PHOSPHORICUM 12X,KALI MURIATICUM 6X,MAGNESIA PHOSPHORICA 6XTalbots Pharmaceuticals Family Products, LLC.e892c0cb-03b4-52da-e053-2995a90a08782022-09-12WarningsExact identifier
unii: 660YQ98I10
POTASSIUM CHLORIDEPOTASSIUM CHLORIDEDr. Reddys Laboratories, Inc.dda82a38-0c08-4947-99b7-915c2949bf162022-08-29Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Potassium ChloridePOTASSIUM CHLORIDEActavis Pharma, Inc.db002ae3-f54c-40a4-9cb4-e5681bf426e32022-08-01Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Potassium ChloridePOTASSIUM CHLORIDEActavis Pharma, Inc.ed5baaf6-270b-4dd3-b100-36030c0098fc2022-08-01Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10

Reported adverse events (FAERS/openFDA)#

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