NDC 60760-200

Oxycodone Hydrochloride and Acetaminophen

Oxycodone Hydrochloride And Acetaminophen

Oxycodone Hydrochloride and Acetaminophen is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by St. Mary's Medical Park Pharmacy. The primary component is Oxycodone Hydrochloride; Acetaminophen.

Product ID60760-200_7b20c416-522e-737a-e053-2991aa0a5709
NDC60760-200
Product TypeHuman Prescription Drug
Proprietary NameOxycodone Hydrochloride and Acetaminophen
Generic NameOxycodone Hydrochloride And Acetaminophen
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2009-06-08
Marketing CategoryANDA / ANDA
Application NumberANDA040777
Labeler NameSt. Mary's Medical Park Pharmacy
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 Through2019-12-31

Packaging

NDC 60760-200-30

30 TABLET in 1 BOTTLE, PLASTIC (60760-200-30)
Marketing Start Date2009-06-08
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 60760-200-30 [60760020030]

Oxycodone Hydrochloride and Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA040777
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-06-08
Marketing End Date2018-01-31

NDC 60760-200-20 [60760020020]

Oxycodone Hydrochloride and Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA040777
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-06-08
Marketing End Date2017-12-07

NDC 60760-200-10 [60760020010]

Oxycodone Hydrochloride and Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA040777
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-06-08
Marketing End Date2017-12-07

NDC 60760-200-60 [60760020060]

Oxycodone Hydrochloride and Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA040777
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-06-08
Marketing End Date2018-08-31

NDC 60760-200-40 [60760020040]

Oxycodone Hydrochloride and Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA040777
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-06-08
Marketing End Date2018-03-31

NDC 60760-200-92 [60760020092]

Oxycodone Hydrochloride and Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA040777
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-06-08
Marketing End Date2017-12-07

NDC 60760-200-90 [60760020090]

Oxycodone Hydrochloride and Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA040777
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-06-08
Marketing End Date2017-12-07

Drug Details

Active Ingredients

IngredientStrength
OXYCODONE HYDROCHLORIDE5 mg/1

OpenFDA Data

SPL SET ID:b43d7ece-d41f-4955-944c-416f479c5cc6
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1049221

    • Pharmacological Class

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

    NDC Crossover Matching brand name "Oxycodone Hydrochloride and Acetaminophen" or generic name "Oxycodone Hydrochloride And Acetaminophen"

    NDCBrand NameGeneric Name
    29033-405Oxycodone Hydrochloride and AcetaminophenOxycodone Hydrochloride and Acetaminophen
    46672-648oxycodone hydrochloride and acetaminophenoxycodone hydrochloride and acetaminophen
    60760-200Oxycodone Hydrochloride and AcetaminophenOxycodone Hydrochloride and Acetaminophen
    64850-622Oxycodone Hydrochloride and AcetaminophenOxycodone Hydrochloride and Acetaminophen
    64850-623Oxycodone Hydrochloride and AcetaminophenOxycodone Hydrochloride and Acetaminophen
    64850-621Oxycodone Hydrochloride and AcetaminophenOxycodone Hydrochloride and Acetaminophen
    72887-648oxycodone hydrochloride and acetaminophenoxycodone hydrochloride and acetaminophen
    0406-0512OXYCODONE AND ACETAMINOPHENoxycodone hydrochloride and acetaminophen
    0406-0522OXYCODONE AND ACETAMINOPHENoxycodone hydrochloride and acetaminophen
    0406-0523OXYCODONE AND ACETAMINOPHENoxycodone hydrochloride 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
    0904-6437Oxycodone and AcetaminophenOxycodone hydrochloride and Acetaminophen
    0904-6438Oxycodone and AcetaminophenOxycodone hydrochloride and Acetaminophen
    0904-6439Oxycodone and AcetaminophenOxycodone hydrochloride and Acetaminophen
    10544-287OXYCODONE AND ACETAMINOPHENoxycodone hydrochloride and acetaminophen
    21695-233OXYCODONE AND ACETAMINOPHENoxycodone hydrochloride and acetaminophen
    21695-616Oxycodone and AcetaminophenOxycodone hydrochloride and Acetaminophen
    52959-556Oxycodone and AcetaminophenOxycodone hydrochloride and Acetaminophen
    55700-983OXYCODONE AND ACETAMINOPHENoxycodone hydrochloride and acetaminophen
    55700-984OXYCODONE AND ACETAMINOPHENoxycodone hydrochloride and acetaminophen
    63187-406Oxycodone and AcetaminophenOxycodone hydrochloride and Acetaminophen
    63481-623PERCOCEToxycodone hydrochloride and acetaminophen
    63481-627PERCOCEToxycodone hydrochloride and acetaminophen
    23635-115Xartemisoxycodone hydrochloride and acetaminophen
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