NDC 53489-110

Carisoprodol

Carisoprodol

Carisoprodol is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Mutual Pharmaceutical Company, Inc.. The primary component is Carisoprodol.

Product ID53489-110_cdfbe64d-ba89-4cb7-bc1a-3bfaadd0258c
NDC53489-110
Product TypeHuman Prescription Drug
Proprietary NameCarisoprodol
Generic NameCarisoprodol
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1991-10-17
Marketing CategoryANDA / ANDA
Application NumberANDA089346
Labeler NameMutual Pharmaceutical Company, Inc.
Substance NameCARISOPRODOL
Active Ingredient Strength350 mg/1
Pharm ClassesCentrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]
DEA ScheduleCIV
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 53489-110-01

100 TABLET in 1 BOTTLE, PLASTIC (53489-110-01)
Marketing Start Date1991-10-17
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 53489-110-01 [53489011001]

Carisoprodol TABLET
Marketing CategoryANDA
Application NumberANDA089346
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1991-10-17
Inactivation Date2019-11-27

NDC 53489-110-05 [53489011005]

Carisoprodol TABLET
Marketing CategoryANDA
Application NumberANDA089346
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1991-10-17
Inactivation Date2019-11-27

NDC 53489-110-60 [53489011060]

Carisoprodol TABLET
Marketing CategoryANDA
Application NumberANDA089346
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1991-10-17
Inactivation Date2019-11-27

NDC 53489-110-06 [53489011006]

Carisoprodol TABLET
Marketing CategoryANDA
Application NumberANDA089346
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1991-10-17
Inactivation Date2019-11-27

NDC 53489-110-10 [53489011010]

Carisoprodol TABLET
Marketing CategoryANDA
Application NumberANDA089346
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1991-10-17
Inactivation Date2019-11-27

NDC 53489-110-07 [53489011007]

Carisoprodol TABLET
Marketing CategoryANDA
Application NumberANDA089346
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1991-10-17
Inactivation Date2019-11-27

Drug Details

Active Ingredients

IngredientStrength
CARISOPRODOL350 mg/1

OpenFDA Data

SPL SET ID:76a36c15-38d3-442e-84a0-b0649a213d13
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197446

    • Pharmacological Class

    • Centrally-mediated Muscle Relaxation [PE]
    • Muscle Relaxant [EPC]

    NDC Crossover Matching brand name "Carisoprodol" or generic name "Carisoprodol"

    NDCBrand NameGeneric Name
    0143-1176CarisoprodolCarisoprodol
    0143-9749CarisoprodolCarisoprodol
    0591-5513CarisoprodolCarisoprodol
    0603-2582CarisoprodolCarisoprodol
    10544-033CarisoprodolCarisoprodol
    10544-088CARISOPRODOLCARISOPRODOL
    10544-132CarisoprodolCarisoprodol
    12634-437CarisoprodolCarisoprodol
    16571-780carisoprodolcarisoprodol
    16571-781carisoprodolcarisoprodol
    16714-510CarisoprodolCarisoprodol
    29033-207CarisoprodolCarisoprodol
    29033-214CarisoprodolCarisoprodol
    33261-387CarisoprodolCarisoprodol
    33358-064CARISOPRODOLCARISOPRODOL
    35356-721CarisoprodolCarisoprodol
    42254-068CarisoprodolCarisoprodol
    42543-434CARISOPRODOLCARISOPRODOL
    42543-700CARISOPRODOLCARISOPRODOL
    43063-302CarisoprodolCarisoprodol
    43063-824CarisoprodolCarisoprodol
    43353-102CARISOPRODOLCARISOPRODOL
    68071-2188CarisoprodolCarisoprodol
    68071-4263CarisoprodolCarisoprodol
    68071-4112CarisoprodolCarisoprodol
    68071-4610CARISOPRODOLCARISOPRODOL
    68387-600CarisoprodolCarisoprodol
    68788-6866CarisoprodolCarisoprodol
    68788-2582CarisoprodolCarisoprodol
    68788-9976CARISOPRODOLCARISOPRODOL
    70518-0704CarisoprodolCarisoprodol
    70518-1092CarisoprodolCarisoprodol
    70518-1401CarisoprodolCarisoprodol
    71335-0131CarisoprodolCarisoprodol
    71205-241CARISOPRODOLCARISOPRODOL
    71335-0407CarisoprodolCarisoprodol
    71335-0516CARISOPRODOLCARISOPRODOL
    71335-0693CARISOPRODOLCARISOPRODOL
    71610-097CARISOPRODOLCARISOPRODOL
    75921-513CARISOPRODOLCARISOPRODOL
    76333-135CarisoprodolCarisoprodol
    50090-0281CarisoprodolCarisoprodol
    49999-064CarisoprodolCarisoprodol
    50090-0280CarisoprodolCarisoprodol
    50090-2530CarisoprodolCarisoprodol
    50090-3232CarisoprodolCarisoprodol
    50090-3048CARISOPRODOLCARISOPRODOL
    50090-3211CarisoprodolCarisoprodol
    50090-2771CarisoprodolCarisoprodol
    50228-109CARISOPRODOLCARISOPRODOL
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.