NDC 51688-9282 - A3265-18 SINGLE SHOT EPIDURAL

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
51688-9282
Package NDCs from labels
51688-9282-2
Manufacturer
Smiths Medical ASD, Inc. | Hospira, Inc. | Kwang Myung Pharm. Co., Ltd.
Effective date
2016-07-08
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
A3265-18 SINGLE SHOT EPIDURALSmiths Medical ASD, Inc. | Hospira, Inc. | Kwang Myung Pharm. Co., Ltd.2016-07-08MEDICAL DEVICE

DailyMed Socrata Ingredients#

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 69 of 86 · 1,702 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEMedical Purchasing Solutions, LLC0a353fe1-b779-3d1f-e063-6294a90ab21b2023-11-15Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
Totally Fun After SunLIDOCAINE HCLMJ Products Association, LLC965a2a29-914c-4ad0-b25f-5df3c30da3932023-11-15WarningsExact identifier
unii: V13007Z41A
Muriaticum acidumHYDROCHLORIC ACIDBoiron8643994f-4e13-4572-e053-2991aa0a5b782023-11-14Exact identifier
unii: QTT17582CB
Muriaticum acidumHYDROCHLORIC ACIDBoiron6907bbfe-caa5-2ce4-e053-2991aa0ade8d2023-11-14Exact identifier
unii: QTT17582CB
Muriaticum acidumHYDROCHLORIC ACIDBoiron8643c518-13b2-658a-e053-2a91aa0ac5ed2023-11-14Exact identifier
unii: QTT17582CB
Muriaticum acidumHYDROCHLORIC ACIDBoiron8643e30e-1f47-09f1-e053-2991aa0ac2de2023-11-14Exact identifier
unii: QTT17582CB
Natrum muriaticumSODIUM CHLORIDEBoiron8646d7ea-cf5e-607d-e053-2a91aa0aeca12023-11-14Exact identifier
unii: 451W47IQ8X
Natrum muriaticumSODIUM CHLORIDEBoiron86466121-7217-d053-e053-2a91aa0a8f8a2023-11-14Exact identifier
unii: 451W47IQ8X
Natrum muriaticumSODIUM CHLORIDEBoiron864669c9-5bdc-232f-e053-2a91aa0a1fc62023-11-14Exact identifier
unii: 451W47IQ8X
Natrum muriaticumSODIUM CHLORIDEBoiron86462e06-d221-36b7-e053-2991aa0a1d822023-11-14Exact identifier
unii: 451W47IQ8X
LidozenLIDOCAINE HYDROCHLORIDE, MENTHOLVillage Pharma, LLC55108ffd-d6a8-41de-e054-00144ff88e882023-11-11WarningsExact identifier
unii: V13007Z41A
MAXOCAINE Lidocaine Hemp Oil Topical AnalgesicLIDOCAINE HYDROCHLORIDEPrime Commerce, LLC28ed2149-38d2-4062-8442-990a98a69cfc2023-11-11WarningsExact identifier
unii: V13007Z41A
MAXOCAINE PAIN RELIEVING ROLL-ONLIDOCAINE HYDROCHLORIDE, MENTHOLPrime Commerce, LLCc263d5f2-89b9-4dfd-91c8-f894e5f956c92023-11-11WarningsExact identifier
unii: V13007Z41A
SUGAR BRANDS Rescue Pain Relief and RecoveryLIDOCAINE HYDROCHLORIDESugar Brands, LLC74013709-d1d5-4425-825d-eee726718c612023-11-11WarningsExact identifier
unii: V13007Z41A
NATURES CRAFT LIDOCAINE Male Genital DesensitizerLIDOCAINE HYDROCHLORIDENatures Design Products LLC61bf1776-5c6c-4307-8348-41fa601640172023-11-11WarningsExact identifier
unii: V13007Z41A
KARMA RUB Elemental Pain ReliefLIDOCAINE HYDROCHLORIDEElemental Bliss LLCc224fb1b-827f-461e-a58f-4020700c3e0d2023-11-11WarningsExact identifier
unii: V13007Z41A
INTIMALE Maximum Strength DelayLIDOCAINE HYDROCHLORIDESKINS SEXUAL HEALTH LIMITED25b9ade3-72b0-4b86-8c48-90310a26806f2023-11-11WarningsExact identifier
unii: V13007Z41A
POWERECT Max Power Male DelayLIDOCAINE HYDROCHLORIDESKINS SEXUAL HEALTH LIMITED25a1c926-9543-44a7-865e-a4b6e1a40cbe2023-11-11WarningsExact identifier
unii: V13007Z41A
SKINS DELAY Maximum Strength LidocaineLIDOCAINE HYDROCHLORIDESKINS SEXUAL HEALTH LIMITED172efe5d-28b8-443c-b3f9-4296691890812023-11-11WarningsExact identifier
unii: V13007Z41A
LIDOSOLVE PAIN RELIEFLIDOCAINE HYDROCHLORIDEHENNIKA HEALTH, LLC3a9e4e0c-362d-4e66-bb5f-984fe1c9d4e22023-11-11WarningsExact identifier
unii: V13007Z41A

Reported adverse events (FAERS/openFDA)#

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