FDA.reportPublic FDA data

NDC 42023-237-01 - Vasostrict

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
42023-237
Requested NDC
42023-237-01
Package NDCs from labels
42023-237-01, 42023-237-10
Manufacturer
Par Health USA, LLC
Effective date
2026-04-21
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Vasostrict - Par Health USA, LLCPar Health USA, LLC2026-04-21HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
42023-237-01Vasostrict100 mL in 1 VIALINJECTION10049
42023-237-10Vasostrict10 in 1 CARTONINJECTION1049

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
42023-237VASOSTRICT (VASOPRESSIN) INJECTION [ENDO USA, INC.]43Current NDC, Legacy NDC, 2 package rows20240425_b1147beb-743e-4c62-8927-91192447f8b8.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
42023-237-01ML - Milliliter42023-237b988a98b-c762-4f6c-8379-b55069082cd612022-03-09
42023-237-10ML - Milliliter42023-2377124f9aa-b422-433c-ba3a-8c7c08c857c212022-03-09

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Vasopressin, UnspecifiedACTIVE INGREDIENTY87Y826H08VASOSTRICT (VASOPRESSIN) INJECTION [PAR PHARMACEUTICAL, INC.]5
Vasopressin, UnspecifiedACTIVE MOIETYY87Y826H08VASOSTRICT (VASOPRESSIN) INJECTION [PAR PHARMACEUTICAL, INC.]5
Acetic acidINACTIVE INGREDIENTQ40Q9N063PVASOSTRICT (VASOPRESSIN) INJECTION [PAR PHARMACEUTICAL, INC.]5
ChlorobutanolINACTIVE INGREDIENTHM4YQM8WRCVASOSTRICT (VASOPRESSIN) INJECTION [PAR PHARMACEUTICAL, INC.]5
WaterINACTIVE INGREDIENT059QF0KO0RVASOSTRICT (VASOPRESSIN) INJECTION [PAR PHARMACEUTICAL, INC.]5

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 17 · 340 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
HepatatoxTRITICUM AESTIVUM, CHELIDONIUM MAJUS, TARAXACUM OFFICINALE, GLUTATHIONE, HEPAR SUIS, THYROIDINUM (SUIS), LYCOPODIUM CLAVATUM, NUX VOMICA, PHOSPHORICUM ACIDUM, ADRENOCORTICOTROPHIN, SALICYLICUM ACIDUM, CORTISONE ACETICUM, EUGENOL, STEARYL ALCOHOL, XYLITOL, FOLLICULINUM, BENZOICUM ACIDUM, CHLORINUM POTASSIUM SORBATE, SORBITOL, RESORCINUM, BENZYL ALCOHOL, LACTICUM ACIDUM, ISOPROPYL PALMITATE, BORICUM ACIDUM, ACETICUM ACIDUM, PHENYL BUTAZONE, PETROLEUM JELLY, PLUMBUM METALLICUMBioActive Nutritional, Inca113a9f1-4792-41a5-8d1b-a6756f356e152025-12-18WarningsExact identifier
unii: Q40Q9N063P
HemorrhoidAESCULUS HIPP, HAMAMELIS, ALOE, CALC PHOS, CARBO AN, CARBO VEG, LACHESIS, LYCOPODIUM, MURIATICUM AC, NITRICUM AC, NUX VOM, PAEONIA, RATANHIA, SEPIA, SULPHURNatural Creations, Incdb1b3aef-ba92-417c-b6f6-58e950ed42142025-12-16WarningsExact identifier
unii: QTT17582CB
Firstep FirstflushEYEWASHEncon Safety Products, Inc.a44beb26-79ae-98bd-e053-2995a90a9b742025-12-09WarningsExact identifier
unii: 059QF0KO0R
Anti Nausea Liquid Cherry FlavorDEXTROSE(GLUCOSE),LEVULOSE(FRUCTOSE),PHOSPHORIC ACIDQUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)743b215a-81cc-408c-9375-4f427161a05b2025-12-04WarningsExact identifier
unii: IY9XDZ35W2
QUALITY CHOICE Anti-NauseaDEXTROSE(GLUCOSE),LEVULOSE(FRUCTOSE),PHOSPHORIC ACIDQUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)68207fa3-3f69-4405-9191-be702e1bf5202025-12-04WarningsExact identifier
unii: IY9XDZ35W2
Walgreen Anti Nausea Cherry FlavorPHOSPHORATED CARBOHYDRATEWALGREENS CO.69e72d30-feca-454d-addc-8ed7325568d32025-12-01WarningsExact identifier
unii: IY9XDZ35W2
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
PUR-WASHWATERNiagara Pharmaceuticals Inc.777e1559-786f-8d54-e053-2991aa0aa98d2025-11-24WarningsExact identifier
unii: 059QF0KO0R
PUR-WASHWATERNiagara Pharmaceuticals Inc.7289103a-5cbf-42f4-8848-e827149a43ca2025-11-24WarningsExact identifier
unii: 059QF0KO0R
Eyewash Additive ConcentrateWATER AND PROPYLENE GLYCOLHaws Corporationdd168403-398c-41ff-b1df-d93e4ff39de32025-11-20WarningsExact identifier
unii: 059QF0KO0R
Sterile WaterWATERFresenius Kabi USA, LLCfd823bef-c14c-4708-a18a-8aaa8470412f2025-11-18Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Eyesaline Eyewash ConcentratePURIFIED WATERHoneywell Safety Products USA, Inc.3765c251-eb14-d60f-e063-6294a90a6a4d2025-11-12WarningsExact identifier
unii: 059QF0KO0R
Eyesaline Emergency EyewashPURIFIED WATERHoneywell Safety Products USA, Inc.37f244fd-c02f-e66a-e063-6394a90aed812025-11-12WarningsExact identifier
unii: 059QF0KO0R
Anti Nausea LiquidPHOSPHORATED CARBOHYDRATETOPCO ASSOCIATES LLCfd0e8feb-89b5-42ff-806a-55b7473cf5872025-11-10WarningsExact identifier
unii: IY9XDZ35W2
STERILE WATERWATERHenry Schein, Inc.f4087143-9868-4308-b96c-43657ee8ec282025-11-07Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
AS-3AS-3GVS TM INC3dfa3397-fc13-4659-e063-6394a90a5abc2025-11-06WarningsExact identifier
unii: IY9XDZ35W2

Reported adverse events (FAERS/openFDA)#

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