NDC 0409-4712

Lidocaine Hydrochloride and Dextrose

Lidocaine Hydrochloride And Dextrose

Lidocaine Hydrochloride and Dextrose is a Intraspinal Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Hospira, Inc.. The primary component is Dextrose Monohydrate; Lidocaine Hydrochloride.

Product ID0409-4712_182e418c-9549-4815-8e91-76c85534f242
NDC0409-4712
Product TypeHuman Prescription Drug
Proprietary NameLidocaine Hydrochloride and Dextrose
Generic NameLidocaine Hydrochloride And Dextrose
Dosage FormInjection, Solution
Route of AdministrationINTRASPINAL
Marketing Start Date2005-06-22
Marketing CategoryANDA / ANDA
Application NumberANDA083914
Labeler NameHospira, Inc.
Substance NameDEXTROSE MONOHYDRATE; LIDOCAINE HYDROCHLORIDE
Active Ingredient Strength75 mg/mL; mg/mL
Pharm ClassesAmide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 0409-4712-01

5 CELLO PACK in 1 PACKAGE (0409-4712-01) > 5 AMPULE in 1 CELLO PACK (0409-4712-25) > 2 mL in 1 AMPULE (0409-4712-11)
Marketing Start Date2005-06-22
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0409-4712-25 [00409471225]

Lidocaine Hydrochloride and Dextrose INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberANDA083914
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-01-11

NDC 0409-4712-01 [00409471201]

Lidocaine Hydrochloride and Dextrose INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberANDA083914
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2005-06-22

NDC 0409-4712-11 [00409471211]

Lidocaine Hydrochloride and Dextrose INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberANDA083914
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2016-06-16

NDC 0409-4712-52 [00409471252]

Lidocaine Hydrochloride and Dextrose INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberANDA083914
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-04-26
Marketing End Date2011-08-16

Drug Details

Active Ingredients

IngredientStrength
LIDOCAINE HYDROCHLORIDE50 mg/mL

OpenFDA Data

SPL SET ID:1f3184a9-8136-4ef1-3590-9ad15c231b26
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1011093
  • Pharmacological Class

    • Amide Local Anesthetic [EPC]
    • Amides [CS]
    • Antiarrhythmic [EPC]
    • Local Anesthesia [PE]

    NDC Crossover Matching brand name "Lidocaine Hydrochloride and Dextrose" or generic name "Lidocaine Hydrochloride And Dextrose"

    NDCBrand NameGeneric Name
    0264-9594Lidocaine Hydrochloride and DextroseLIDOCAINE HYDROCHLORIDE ANHYDROUS and DEXTROSE MONOHYDRATE
    0264-9598Lidocaine Hydrochloride and DextroseLIDOCAINE HYDROCHLORIDE ANHYDROUS and DEXTROSE MONOHYDRATE
    0338-0409Lidocaine Hydrochloride and DextroseLidocaine Hydrochloride
    0338-0411Lidocaine Hydrochloride and DextroseLidocaine Hydrochloride
    0338-9586Lidocaine Hydrochloride and DextroseLidocaine Hydrochloride
    0338-9590Lidocaine Hydrochloride and DextroseLidocaine Hydrochloride
    0409-4712Lidocaine Hydrochloride and Dextroselidocaine hydrochloride and dextrose
    50090-4555Lidocaine Hydrochloride and DextroseLIDOCAINE HYDROCHLORIDE ANHYDROUS and DEXTROSE MONOHYDRATE
    50090-4559Lidocaine Hydrochloride and DextroseLIDOCAINE HYDROCHLORIDE ANHYDROUS and DEXTROSE MONOHYDRATE

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