NDC 68788-7298

LAMIVUDINE and ZIDOVUDINE

Lamivudine And Zidovudine

LAMIVUDINE and ZIDOVUDINE is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is Lamivudine; Zidovudine.

Product ID68788-7298_96a34788-b1f8-4c0c-afc7-e2bfbef59960
NDC68788-7298
Product TypeHuman Prescription Drug
Proprietary NameLAMIVUDINE and ZIDOVUDINE
Generic NameLamivudine And Zidovudine
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2019-01-04
Marketing CategoryANDA / ANDA
Application NumberANDA079124
Labeler NamePreferred Pharmaceuticals Inc.
Substance NameLAMIVUDINE; ZIDOVUDINE
Active Ingredient Strength150 mg/1; mg/1
Pharm ClassesHepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [EXT],Nucleoside Reverse Transcriptase Inhibitors [MoA],Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [EXT],Nucleoside Reverse Transcriptase Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 68788-7298-1

100 TABLET, FILM COATED in 1 BOTTLE (68788-7298-1)
Marketing Start Date2019-01-06
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68788-7298-3 [68788729803]

LAMIVUDINE and ZIDOVUDINE TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA079124
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2019-01-06

NDC 68788-7298-8 [68788729808]

LAMIVUDINE and ZIDOVUDINE TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA079124
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2019-01-06

NDC 68788-7298-6 [68788729806]

LAMIVUDINE and ZIDOVUDINE TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA079124
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2019-01-06

NDC 68788-7298-1 [68788729801]

LAMIVUDINE and ZIDOVUDINE TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA079124
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2019-01-06

NDC 68788-7298-9 [68788729809]

LAMIVUDINE and ZIDOVUDINE TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA079124
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2019-01-06

NDC 68788-7298-4 [68788729804]

LAMIVUDINE and ZIDOVUDINE TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA079124
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2019-01-06

NDC 68788-7298-2 [68788729802]

LAMIVUDINE and ZIDOVUDINE TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA079124
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2019-01-06

Drug Details

Active Ingredients

IngredientStrength
LAMIVUDINE150 mg/1

OpenFDA Data

SPL SET ID:96a34788-b1f8-4c0c-afc7-e2bfbef59960
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 200082

    • Pharmacological Class

    • Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]
    • Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]
    • Nucleoside Analog [EXT]
    • Nucleoside Reverse Transcriptase Inhibitors [MoA]
    • Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]
    • Nucleoside Analog [EXT]
    • Nucleoside Reverse Transcriptase Inhibitors [MoA]

    NDC Crossover Matching brand name "LAMIVUDINE and ZIDOVUDINE" or generic name "Lamivudine And Zidovudine"

    NDCBrand NameGeneric Name
    21695-996Lamivudine and ZidovudineLamivudine and Zidovudine
    31722-506LAMIVUDINE and ZIDOVUDINELAMIVUDINE and ZIDOVUDINE
    31722-739Lamivudine and ZidovudineLamivudine and Zidovudine
    33342-003Lamivudine and ZidovudineLamivudine and Zidovudine
    42291-363Lamivudine and ZidovudineLamivudine and Zidovudine
    43063-346Lamivudine and ZidovudineLamivudine and Zidovudine
    43063-900lamiVUDine and ZIDOVUDINElamiVUDine and ZIDOVUDINE
    50090-3920LAMIVUDINE and ZIDOVUDINELAMIVUDINE and ZIDOVUDINE
    50268-456LAMIVUDINE and ZIDOVUDINELAMIVUDINE and ZIDOVUDINE
    50436-0597Lamivudine and ZidovudineLamivudine and Zidovudine
    54741-102Lamivudine and Zidovudinelamivudine and zidovudine
    55700-096Lamivudine and ZidovudineLamivudine and Zidovudine
    57297-284LAMIVUDINE AND ZIDOVUDINELAMIVUDINE AND ZIDOVUDINE
    63629-4872Lamivudine and ZidovudineLamivudine and Zidovudine
    64380-707Lamivudine and ZidovudineLamivudine and Zidovudine
    65862-036Lamivudine and ZidovudineLamivudine and Zidovudine
    65862-597Lamivudine and ZidovudineLamivudine and Zidovudine
    68071-3311Lamivudine and ZidovudineLamivudine and Zidovudine
    68071-4450LAMIVUDINE and ZIDOVUDINELAMIVUDINE and ZIDOVUDINE
    68084-416Lamivudine and ZidovudineLamivudine and Zidovudine
    68180-284LAMIVUDINE AND ZIDOVUDINELAMIVUDINE AND ZIDOVUDINE
    68788-6394Lamivudine and ZidovudineLamivudine and Zidovudine
    68788-7298LAMIVUDINE and ZIDOVUDINELAMIVUDINE and ZIDOVUDINE
    69097-315Lamivudine and ZidovudineLamivudine and Zidovudine
    70518-0697Lamivudine and ZidovudineLamivudine and Zidovudine
    71335-0141Lamivudine and ZidovudineLamivudine and Zidovudine
    71335-0639LAMIVUDINE and ZIDOVUDINELAMIVUDINE and ZIDOVUDINE
    76519-1005Lamivudine and ZidovudineLamivudine and Zidovudine
    76282-115Lamivudine and ZidovudineLamivudine and Zidovudine
    72865-144LAMIVUDINE AND ZIDOVUDINELAMIVUDINE AND ZIDOVUDINE
    21695-846COMBIVIRlamivudine and zidovudine
    49702-202COMBIVIRlamivudine and zidovudine
    50090-0610COMBIVIRlamivudine and zidovudine
    52959-546COMBIVIRlamivudine and zidovudine
    53808-0895COMBIVIRlamivudine and zidovudine
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