NDC 0406-0512

OXYCODONE AND ACETAMINOPHEN

Oxycodone Hydrochloride And Acetaminophen

OXYCODONE AND ACETAMINOPHEN is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Specgx Llc. The primary component is Oxycodone Hydrochloride; Acetaminophen.

Product ID0406-0512_058431b8-117a-4b0c-bee1-f169391d327c
NDC0406-0512
Product TypeHuman Prescription Drug
Proprietary NameOXYCODONE AND ACETAMINOPHEN
Generic NameOxycodone Hydrochloride And Acetaminophen
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1983-12-07
Marketing CategoryANDA / ANDA
Application NumberANDA087463
Labeler NameSpecGx LLC
Substance NameOXYCODONE HYDROCHLORIDE; ACETAMINOPHEN
Active Ingredient Strength5 mg/1; mg/1
Pharm ClassesFull Opioid Agonists [MoA],Opioid Agonist [EPC]
DEA ScheduleCII
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 0406-0512-01

100 TABLET in 1 BOTTLE (0406-0512-01)
Marketing Start Date1983-12-07
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0406-0512-23 [00406051223]

OXYCODONE AND ACETAMINOPHEN TABLET
Marketing CategoryANDA
Application NumberANDA087463
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1983-12-07

NDC 0406-0512-91 [00406051291]

OXYCODONE AND ACETAMINOPHEN TABLET
Marketing CategoryANDA
Application NumberANDA087463
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1983-12-07

NDC 0406-0512-05 [00406051205]

OXYCODONE AND ACETAMINOPHEN TABLET
Marketing CategoryANDA
Application NumberANDA087463
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1983-12-07

NDC 0406-0512-62 [00406051262]

OXYCODONE AND ACETAMINOPHEN TABLET
Marketing CategoryANDA
Application NumberANDA087463
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1983-12-07

NDC 0406-0512-01 [00406051201]

OXYCODONE AND ACETAMINOPHEN TABLET
Marketing CategoryANDA
Application NumberANDA087463
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1983-12-07

Drug Details

Active Ingredients

IngredientStrength
OXYCODONE HYDROCHLORIDE5 mg/1

OpenFDA Data

SPL SET ID:f2137f1a-b49a-40bd-97ac-cd6b36e295f4
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1049214
  • 1049221
  • 1049225
    • UPC Code
  • 0304060512054
  • 0304060522053
  • 0304060523050

    • Pharmacological Class

    • Full Opioid Agonists [MoA]
    • Opioid Agonist [EPC]

    NDC Crossover Matching brand name "OXYCODONE AND ACETAMINOPHEN" or generic name "Oxycodone Hydrochloride And Acetaminophen"

    NDCBrand NameGeneric Name
    0054-0551Oxycodone and AcetaminophenOxycodone and Acetaminophen
    0228-2981Oxycodone and AcetaminophenOxycodone and Acetaminophen
    0228-2982Oxycodone and AcetaminophenOxycodone and Acetaminophen
    0228-2983Oxycodone and AcetaminophenOxycodone and Acetaminophen
    0406-0512OXYCODONE AND ACETAMINOPHENoxycodone hydrochloride and acetaminophen
    0406-0522OXYCODONE AND ACETAMINOPHENoxycodone hydrochloride and acetaminophen
    0406-0523OXYCODONE AND ACETAMINOPHENoxycodone hydrochloride and acetaminophen
    0527-1669Oxycodone and AcetaminophenOxycodone and Acetaminophen
    0527-1671Oxycodone and AcetaminophenOxycodone and Acetaminophen
    0603-4978Oxycodone and AcetaminophenOxycodone hydrochloride and Acetaminophen
    0603-4979Oxycodone and AcetaminophenOxycodone hydrochloride and Acetaminophen
    0603-4982Oxycodone and AcetaminophenOxycodone hydrochloride and Acetaminophen
    0603-4998Oxycodone and AcetaminophenOxycodone hydrochloride and Acetaminophen
    68084-355Oxycodone and AcetaminophenOxycodone and Acetaminophen
    68084-710Oxycodone and AcetaminophenOxycodone and Acetaminophen
    68094-013Oxycodone and AcetaminophenOxycodone and Acetaminophen
    68084-699Oxycodone and AcetaminophenOxycodone and Acetaminophen
    68308-480Oxycodone and AcetaminophenOxycodone and Acetaminophen
    68308-840Oxycodone and AcetaminophenOxycodone and Acetaminophen
    68308-842Oxycodone and AcetaminophenOxycodone and Acetaminophen
    68308-843Oxycodone and AcetaminophenOxycodone and Acetaminophen
    68308-405Oxycodone and AcetaminophenOxycodone and Acetaminophen
    68308-475Oxycodone and AcetaminophenOxycodone and Acetaminophen
    68308-841Oxycodone and AcetaminophenOxycodone and Acetaminophen
    70700-105Oxycodone and AcetaminophenOxycodone and Acetaminophen
    70710-1327Oxycodone and AcetaminophenOxycodone and Acetaminophen
    70710-1328Oxycodone and AcetaminophenOxycodone and Acetaminophen
    70710-1329Oxycodone and AcetaminophenOxycodone and Acetaminophen
    70710-1330Oxycodone and AcetaminophenOxycodone and Acetaminophen
    71335-0146Oxycodone and AcetaminophenOxycodone and Acetaminophen
    71335-0216Oxycodone and AcetaminophenOxycodone and Acetaminophen
    71335-0193Oxycodone and AcetaminophenOxycodone and Acetaminophen
    71335-0221oxycodone and acetaminophenoxycodone and acetaminophen
    71335-1036Oxycodone and AcetaminophenOxycodone and Acetaminophen
    71335-0316Oxycodone and AcetaminophenOxycodone and Acetaminophen
    71335-0722Oxycodone and AcetaminophenOxycodone and Acetaminophen
    0904-6438Oxycodone and AcetaminophenOxycodone and Acetaminophen
    0904-6439Oxycodone and AcetaminophenOxycodone and Acetaminophen
    0904-6437Oxycodone and AcetaminophenOxycodone and Acetaminophen
    10544-287OXYCODONE AND ACETAMINOPHENOXYCODONE AND ACETAMINOPHEN
    10702-187Oxycodone and AcetaminophenOxycodone and Acetaminophen
    10544-621Oxycodone and AcetaminophenOxycodone and Acetaminophen
    10702-238OXYCODONE AND ACETAMINOPHENOXYCODONE AND ACETAMINOPHEN
    10702-185Oxycodone and AcetaminophenOxycodone and Acetaminophen
    10702-186Oxycodone and AcetaminophenOxycodone and Acetaminophen
    10702-184Oxycodone and AcetaminophenOxycodone and Acetaminophen
    13107-044Oxycodone and AcetaminophenOxycodone and Acetaminophen
    13107-043Oxycodone and AcetaminophenOxycodone and Acetaminophen
    12634-942Oxycodone and AcetaminophenOxycodone and Acetaminophen
    13107-045Oxycodone and AcetaminophenOxycodone and Acetaminophen
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