NDC 0185-0749

Carisoprodol, Aspirin and Codeine Phosphate

Carisoprodol, Aspirin And Codeine Phosphate

Carisoprodol, Aspirin and Codeine Phosphate is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Eon Labs, Inc.. The primary component is Carisoprodol; Aspirin; Codeine Phosphate.

Product ID0185-0749_e1eaeba6-7e4b-4851-9554-8564fc7c4c72
NDC0185-0749
Product TypeHuman Prescription Drug
Proprietary NameCarisoprodol, Aspirin and Codeine Phosphate
Generic NameCarisoprodol, Aspirin And Codeine Phosphate
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1996-04-16
Marketing End Date2019-09-30
Marketing CategoryANDA / ANDA
Application NumberANDA040118
Labeler NameEon Labs, Inc.
Substance NameCARISOPRODOL; ASPIRIN; CODEINE PHOSPHATE
Active Ingredient Strength200 mg/1; mg/1; mg/1
Pharm ClassesCentrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC],Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC],Platelet Aggregation Inhibitor [EPC],Decreased Platelet Aggregation [PE],Full Opioid Agonists [MoA],Opioid Agonist [EPC]
DEA ScheduleCIII
NDC Exclude FlagN

Packaging

NDC 0185-0749-05

500 TABLET in 1 BOTTLE (0185-0749-05)
Marketing Start Date1996-04-16
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0185-0749-05 [00185074905]

Carisoprodol, Aspirin and Codeine Phosphate TABLET
Marketing CategoryANDA
Application NumberANDA040118
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1996-04-16
Marketing End Date2019-09-30

NDC 0185-0749-01 [00185074901]

Carisoprodol, Aspirin and Codeine Phosphate TABLET
Marketing CategoryANDA
Application NumberANDA040118
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1996-04-16
Marketing End Date2019-09-30

NDC 0185-0749-10 [00185074910]

Carisoprodol, Aspirin and Codeine Phosphate TABLET
Marketing CategoryANDA
Application NumberANDA040118
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1996-04-16
Marketing End Date2019-09-30

Drug Details

Active Ingredients

IngredientStrength
CARISOPRODOL200 mg/1

OpenFDA Data

SPL SET ID:dcae7a8a-9d9e-4f7f-954c-39e371f30f75
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 994226
  • Pharm Class PE
  • Decreased Prostaglandin Production [PE]
  • Decreased Platelet Aggregation [PE]
  • PHarm Class EPC
  • Nonsteroidal Anti-inflammatory Drug [EPC]
  • Platelet Aggregation Inhibitor [EPC]
  • NUI Code
  • N0000008832
  • N0000008836
  • N0000175721
  • N0000000160
  • N0000175578
  • N0000175722
  • Pharmacological Class

    • Centrally-mediated Muscle Relaxation [PE]
    • Muscle Relaxant [EPC]
    • Cyclooxygenase Inhibitors [MoA]
    • Decreased Prostaglandin Production [PE]
    • Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient]
    • Nonsteroidal Anti-inflammatory Drug [EPC]
    • Platelet Aggregation Inhibitor [EPC]
    • Decreased Platelet Aggregation [PE]
    • Full Opioid Agonists [MoA]
    • Opioid Agonist [EPC]

    NDC Crossover Matching brand name "Carisoprodol, Aspirin and Codeine Phosphate" or generic name "Carisoprodol, Aspirin And Codeine Phosphate"

    NDCBrand NameGeneric Name
    0185-0749Carisoprodol, Aspirin and Codeine PhosphateCarisoprodol, Aspirin and Codeine Phosphate
    50742-256CARISOPRODOL, ASPIRIN AND CODEINE PHOSPHATEcarisoprodol, aspirin and codeine phosphate
    64980-176Carisoprodol, Aspirin and Codeine PhosphateCarisoprodol, Aspirin and Codeine Phosphate

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