FDA.reportPublic FDA data

NDC 0409-1105-22 - Atracurium Besylate

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
0409-1105
Requested NDC
0409-1105-22
Package NDCs from labels
0409-1105-22, 0409-1105-02
Manufacturer
Hospira, Inc.
Effective date
2023-11-23
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
ATRACURIUM BESYLATE INJECTION USPHospira, Inc.2023-11-23HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0409-1105-02Atracurium Besylate10 in 1 CARTONINJECTION, SOLUTION1012
0409-1105-22Atracurium Besylate10 mL in 1 VIAL, MULTI-DOSEINJECTION, SOLUTION1012

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0409-1105ATRACURIUM BESYLATE INJECTION, SOLUTION [HOSPIRA, INC.]12Current NDC, Legacy NDC, 2 package rows20231125_de1c2dcd-295b-47ce-b7a1-a8be59939a54.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0409-1105-02ML - Milliliter0409-1105847509b0-a5ea-49c8-81d7-46083755fdce12013-07-02
0409-1105-22ML - Milliliter0409-110588bb696b-d3e8-4565-a2f5-088efca2cd7c12019-07-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ATRACURIUM BESYLATEACTIVE INGREDIENT40AX66P76PATRACURIUM BESYLATE INJECTION, SOLUTION [HOSPIRA, INC.]1
ATRACURIUMACTIVE MOIETY2GQ1IRY63PATRACURIUM BESYLATE INJECTION, SOLUTION [HOSPIRA, INC.]1
BENZENESULFONIC ACIDINACTIVE INGREDIENT685928Z18AATRACURIUM BESYLATE INJECTION, SOLUTION [HOSPIRA, INC.]1
BENZYL ALCOHOLINACTIVE INGREDIENTLKG8494WBHATRACURIUM BESYLATE INJECTION, SOLUTION [HOSPIRA, INC.]1

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 2 of 2 · 33 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CVS Health Lidocaine Plus Pain RelievingLIDOCAINE HYDROCHLORIDE, BENZYL ALCOHOLNATURAL ESSENTIALS, INC.1adb9b74-4a01-4461-b845-f3aedcb3f8102024-10-01WarningsExact identifier
unii: LKG8494WBH
IvarestZINC OXIDE, BENZYL ALCOHOL, AND DIPHENHYDRAMINE HYDROCHLORIDEBlistex Inc6f68cbbb-6269-4bb3-8cc9-50b146703b422024-07-09WarningsExact identifier
unii: LKG8494WBH
Walgreens Lidocaine Plus CreamBENZYL ALCOHOL AND LIDOCAINE HYDROCHLORIDEWalgreens Companye33e0097-31d6-8083-e053-2a95a90af5d22024-05-09WarningsExact identifier
unii: LKG8494WBH
HealthWise Lidocaine Plus CreamBENZYL ALCOHOL, LIDOCAINE HYDROCHLORIDEVeridian Healthcare16f26249-b508-2c6e-e063-6394a90a265b2024-04-25WarningsExact identifier
unii: LKG8494WBH
CVS Maximum Strength LIDOCAINE PLUSBENZYL ALCOHOL, LIDOCAINE HYDROCHLORIDECVS Pharmacy Inc.e6aff579-affb-41bb-8e36-53ea484cb0c52023-11-26WarningsExact identifier
unii: LKG8494WBH
Atracurium BesylateATRACURIUM BESYLATEHospira, Inc.de1c2dcd-295b-47ce-b7a1-a8be59939a542023-11-23Warnings, Adverse reactionsExact identifier
application number: ANDA090782
application number: ANDA090761
ndc (package): 0409-1105-22
ndc (package): 0409-1109-11
ndc (package): 0409-1109-01
ndc (package): 0409-1105-02
ndc (product): 0409-1109
ndc (product): 0409-1105
ndc11 (package): 00409110522
rxcui: 1718913
rxcui: 966768
spl id: 926d60c7-8585-42f2-a9fc-02fcb51dc2ae
spl set id: de1c2dcd-295b-47ce-b7a1-a8be59939a54
unii: 40AX66P76P
LipotoxSQUALENE, CHOLESTERINUM, ESTRADIOL, PROGESTERONE, ASPARTAME, BENZALKONIUM CHLORIDE, FORMALINUM, METHYLENE CHLORIDE, METHYLPARABEN, PROPYLPARABEN, SODIUM BENZOATE, SODIUM CITRATE, TITANIUM DIOXIDE, ZINCUM OXYDATUM, ARSENICUM ALBUM, LYCOPODIUM CLAVATUM, NUX VOMICA, PHOSPHORICUM ACIDUM, PHOSPHORUS, ACETICUM ACIDUM, BENZOICUM ACIDUM, BENZYL ALCOHOL, BORICUM ACIDUM, CHLORINUM, CORTISONE ACETICUM, EUGENOL, FOLLICULINUM, ISOPROPYL PALMITATE, LACTICUM ACIDUM, PETROLEUM JELLY, PHENYL BUTAZONE, PLUMBUM METALLICUM,BioActive Nutritional, Inc.a1538692-ca00-4e52-9b7e-409767ee27e12023-09-05WarningsExact identifier
unii: LKG8494WBH
Anubis BarcelonaDMAE, ZIRHAFIRMANUBIS COSMETICS SLf2274f8c-08aa-eb02-e053-2a95a90a39982023-09-01WarningsExact identifier
unii: LKG8494WBH
Anubis BarcelonaPROPANEDIOL, GLYCERIN, MAGNESIUM ASCORBYL PHOSPHATEANUBIS COSMETICS SLeb53cba1-0509-43bc-e053-2995a90a5e092023-09-01WarningsExact identifier
unii: LKG8494WBH
Atracurium BesylateATRACURIUM BESYLATEAuroMedics Pharma LLC71d4bc78-57df-474b-8b19-811a959f1fce2022-05-30Warnings, Adverse reactionsExact identifier
rxcui: 1718913
unii: 40AX66P76P
Atracurium BesylateATRACURIUM BESYLATEAuroMedics Pharma LLCf7b6a720-05a7-4d6a-9200-21bdc90fc1c42022-02-14Warnings, Adverse reactionsExact identifier
rxcui: 966768
unii: 40AX66P76P
Ivy-Dry SuperBENZYL ALCOHOL, CAMPHOR, MENTHOLIvy-Dry, Inc.4792a667-2378-4b3d-968d-9efb1866792f2017-12-27WarningsExact identifier
unii: LKG8494WBH
Homeoplex DGLYCERINUM, PHYTOLACCA DECANDRA, TARAXACUM OFFICINALE, ARSENICUM ALBUM, NITRICUM ACIDUM, NUX VOMICA, PETROLEUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, ACETYLSALICYLICUM ACIDUM, GLONOINUM, INSULINUM (SUIS), LITHIUM CARBONICUM, THYROIDINUM (SUIS), SALICYLICUM ACIDUM, ADRENOCORTICOTROPHIN, CORTISONE ACETICUM, EUGENOL, STEARYL ALCOHOL, XYLITOL, FOLLICULINUM, BENZOICUM ACIDUM, CHLORINUM, POTASSIUM SORBATE, SORBITOL, RESORCINUM, BENZYL ALCOHOL, LACTICUM ACIDUM, ISOPROPYL PALMITATE, BORICUM ACIDUM, ACETICUM ACIDUM,Supplement Clinic, LLC.cd6b48ab-3566-484d-8deb-15ef6f8e7e8f2017-11-01WarningsExact identifier
unii: LKG8494WBH

Reported adverse events (FAERS/openFDA)#

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