NDC 63629-3776

PERCOCET

Oxycodone Hydrochloride And Acetaminophen

PERCOCET is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Oxycodone Hydrochloride; Acetaminophen.

Product ID63629-3776_6a486e80-1f8b-4bb8-962f-2bf70ad48a0c
NDC63629-3776
Product TypeHuman Prescription Drug
Proprietary NamePERCOCET
Generic NameOxycodone Hydrochloride And Acetaminophen
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1999-07-30
Marketing CategoryANDA / ANDA
Application NumberANDA040341
Labeler NameBryant Ranch Prepack
Substance NameOXYCODONE HYDROCHLORIDE; ACETAMINOPHEN
Active Ingredient Strength10 mg/1; mg/1
Pharm ClassesFull Opioid Agonists [MoA],Opioid Agonist [EPC]
DEA ScheduleCII
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 63629-3776-6

25 TABLET in 1 BOTTLE (63629-3776-6)
Marketing Start Date1999-07-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63629-3776-6 [63629377606]

PERCOCET TABLET
Marketing CategoryANDA
Application NumberANDA040341
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1999-07-30
Inactivation Date2019-11-27

NDC 63629-3776-5 [63629377605]

PERCOCET TABLET
Marketing CategoryANDA
Application NumberANDA040341
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1999-07-30
Inactivation Date2019-11-27

NDC 63629-3776-2 [63629377602]

PERCOCET TABLET
Marketing CategoryANDA
Application NumberANDA040341
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1999-07-30
Inactivation Date2019-11-27

NDC 63629-3776-1 [63629377601]

PERCOCET TABLET
Marketing CategoryANDA
Application NumberANDA040341
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1999-07-30
Inactivation Date2019-11-27

NDC 63629-3776-3 [63629377603]

PERCOCET TABLET
Marketing CategoryANDA
Application NumberANDA040341
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1999-07-30
Inactivation Date2019-11-27

NDC 63629-3776-4 [63629377604]

PERCOCET TABLET
Marketing CategoryANDA
Application NumberANDA040341
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1999-07-30
Inactivation Date2019-11-27

Drug Details

Active Ingredients

IngredientStrength
OXYCODONE HYDROCHLORIDE10 mg/1

OpenFDA Data

SPL SET ID:d230e95e-5d20-9d06-e710-5410240c301a
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1049270
  • 1049650

    • Pharmacological Class

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

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

    NDCBrand NameGeneric Name
    63481-623PERCOCEToxycodone hydrochloride and acetaminophen
    63481-627PERCOCEToxycodone hydrochloride and acetaminophen
    63481-628PERCOCETPERCOCET
    63481-629PERCOCETPERCOCET
    63629-3773PERCOCETPERCOCET
    63629-3776PERCOCETPERCOCET
    65084-298PERCOCETPERCOCET
    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
    29033-405Oxycodone Hydrochloride and AcetaminophenOxycodone Hydrochloride and Acetaminophen
    46672-648oxycodone hydrochloride and acetaminophenoxycodone hydrochloride and acetaminophen
    60760-200Oxycodone Hydrochloride and AcetaminophenOxycodone Hydrochloride and Acetaminophen
    23635-115Xartemisoxycodone hydrochloride and acetaminophen

    Trademark Results [PERCOCET]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    PERCOCET
    PERCOCET
    73072165 1051682 Live/Registered
    ENDO LABORATORIES, INC.
    1975-12-18
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