NDC 66336-442

Hydrocodone Bitartrate And Acetaminophen

Hydrocodone Bitartrate And Acetaminophen

Hydrocodone Bitartrate And Acetaminophen is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Dispensing Solutions, Inc.. The primary component is Hydrocodone Bitartrate; Acetaminophen.

Product ID66336-442_c2b43b77-8ebb-4559-aaae-2d17741bce3e
NDC66336-442
Product TypeHuman Prescription Drug
Proprietary NameHydrocodone Bitartrate And Acetaminophen
Generic NameHydrocodone Bitartrate And Acetaminophen
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1988-12-02
Marketing CategoryANDA / ANDA
Application NumberANDA089971
Labeler NameDispensing Solutions, Inc.
Substance NameHYDROCODONE BITARTRATE; ACETAMINOPHEN
Active Ingredient Strength5 mg/1; mg/1
Pharm ClassesOpioid Agonist [EPC],Opioid Agonists [MoA]
DEA ScheduleCIII
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 66336-442-06

6 TABLET in 1 BOTTLE, PLASTIC (66336-442-06)
Marketing Start Date1988-12-02
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 66336-442-90 [66336044290]

Hydrocodone Bitartrate And Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA089971
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1988-12-02
Inactivation Date2019-11-27

NDC 66336-442-20 [66336044220]

Hydrocodone Bitartrate And Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA089971
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1988-12-02
Inactivation Date2019-11-27

NDC 66336-442-40 [66336044240]

Hydrocodone Bitartrate And Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA089971
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1988-12-02
Inactivation Date2019-11-27

NDC 66336-442-16 [66336044216]

Hydrocodone Bitartrate And Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA089971
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1988-12-02
Inactivation Date2019-11-27

NDC 66336-442-30 [66336044230]

Hydrocodone Bitartrate And Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA089971
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1988-12-02
Inactivation Date2019-11-27

NDC 66336-442-15 [66336044215]

Hydrocodone Bitartrate And Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA089971
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1988-12-02
Inactivation Date2019-11-27

NDC 66336-442-10 [66336044210]

Hydrocodone Bitartrate And Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA089971
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1988-12-02
Inactivation Date2019-11-27

NDC 66336-442-14 [66336044214]

Hydrocodone Bitartrate And Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA089971
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1988-12-02
Inactivation Date2019-11-27

NDC 66336-442-06 [66336044206]

Hydrocodone Bitartrate And Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA089971
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1988-12-02
Inactivation Date2019-11-27

NDC 66336-442-24 [66336044224]

Hydrocodone Bitartrate And Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA089971
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1988-12-02
Inactivation Date2019-11-27

NDC 66336-442-12 [66336044212]

Hydrocodone Bitartrate And Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA089971
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1988-12-02
Inactivation Date2019-11-27

NDC 66336-442-94 [66336044294]

Hydrocodone Bitartrate And Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA089971
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1988-12-02
Inactivation Date2019-11-27

NDC 66336-442-44 [66336044244]

Hydrocodone Bitartrate And Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA089971
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1988-12-02
Inactivation Date2019-11-27

NDC 66336-442-60 [66336044260]

Hydrocodone Bitartrate And Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA089971
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1988-12-02
Inactivation Date2019-11-27

NDC 66336-442-45 [66336044245]

Hydrocodone Bitartrate And Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA089971
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-08-19
Inactivation Date2019-11-27

Drug Details

Active Ingredients

IngredientStrength
HYDROCODONE BITARTRATE5 mg/1

OpenFDA Data

SPL SET ID:1b733f85-dafb-4242-be8a-65540d956380
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 856903
  • Pharmacological Class

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

    NDC Crossover Matching brand name "Hydrocodone Bitartrate And Acetaminophen" or generic name "Hydrocodone Bitartrate And Acetaminophen"

    NDCBrand NameGeneric Name
    0121-0772Hydrocodone Bitartrate and AcetaminophenHYDROCODONE BITARTRATE and ACETAMINOPHEN
    0121-1544Hydrocodone Bitartrate and AcetaminophenHYDROCODONE BITARTRATE and ACETAMINOPHEN
    0121-2316Hydrocodone Bitartrate and AcetaminophenHYDROCODONE BITARTRATE and ACETAMINOPHEN
    0121-4772Hydrocodone Bitartrate and AcetaminophenHYDROCODONE BITARTRATE and ACETAMINOPHEN
    0245-0410Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen
    68071-4801Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen
    68084-895Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen
    68084-884Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen
    68084-863Hydrocodone Bitartrate And AcetaminophenHydrocodone Bitartrate And Acetaminophen
    68094-714Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen
    68387-230HYDROCODONE BITARTRATE AND ACETAMINOPHENHYDROCODONE BITARTRATE AND ACETAMINOPHEN
    68387-235Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen
    68788-6352Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen
    68788-9137Hydrocodone Bitartrate And AcetaminophenHydrocodone Bitartrate And Acetaminophen
    68788-9141Hydrocodone Bitartrate And AcetaminophenHydrocodone Bitartrate And Acetaminophen
    68788-9125Hydrocodone Bitartrate And AcetaminophenHydrocodone Bitartrate And Acetaminophen
    68788-9297Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen
    68788-9250Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen
    0527-1647Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen
    0527-1649Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen
    0527-1648Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen
    0527-1651Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen
    0527-1646Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen
    0527-1650Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen
    69101-600HYDROCODONE BITARTRATE and ACETAMINOPHENHYDROCODONE BITARTRATE and ACETAMINOPHEN
    0591-2174Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen
    0591-2175Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen
    0591-2171Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen
    0591-2605Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen
    0591-2612Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen
    0591-2172Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen
    0591-2176Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen
    0603-3887Hydrocodone Bitartrate And AcetaminophenHydrocodone Bitartrate And Acetaminophen
    0603-3890Hydrocodone Bitartrate And AcetaminophenHydrocodone Bitartrate And Acetaminophen
    0603-3891Hydrocodone Bitartrate And AcetaminophenHydrocodone Bitartrate And Acetaminophen
    71335-0063HYDROCODONE BITARTRATE AND ACETAMINOPHENHYDROCODONE BITARTRATE AND ACETAMINOPHEN
    71335-0108Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen
    71335-0385HYDROCODONE BITARTRATE AND ACETAMINOPHENHYDROCODONE BITARTRATE AND ACETAMINOPHEN
    71335-0466Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen
    71335-0960Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen
    71930-020Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen
    71930-019Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen
    71930-021Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen
    76519-1079HYDROCODONE BITARTRATE AND ACETAMINOPHENHYDROCODONE BITARTRATE AND ACETAMINOPHEN
    75921-881Hydrocodone Bitartrate And AcetaminophenHydrocodone Bitartrate And Acetaminophen
    76519-1081HYDROCODONE BITARTRATE AND ACETAMINOPHENHYDROCODONE BITARTRATE AND ACETAMINOPHEN
    0713-0704Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen
    0904-6421Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen
    0904-6420Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen
    0904-6567Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophen

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.