NDC 0074-1052

Lupaneta Pack

Leuprolide Acetate And Norethindrone Acetate

Lupaneta Pack is a Kit in the Human Prescription Drug category. It is labeled and distributed by Abbvie Inc.. The primary component is .

Product ID0074-1052_7c0c2326-7ff7-41b2-a441-5b8b6a7a89fe
NDC0074-1052
Product TypeHuman Prescription Drug
Proprietary NameLupaneta Pack
Generic NameLeuprolide Acetate And Norethindrone Acetate
Dosage FormKit
Marketing Start Date2013-07-01
Marketing CategoryNDA / NDA
Application NumberNDA203696
Labeler NameAbbVie Inc.
Active Ingredient Strength0
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 0074-1052-05

1 KIT in 1 CARTON (0074-1052-05) * 1 mL in 1 SYRINGE * 1 mL in 1 PACKET * 30 TABLET in 1 BOTTLE
Marketing Start Date2013-07-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0074-1052-05 [00074105205]

Lupaneta Pack KIT
Marketing CategoryNDA
Application NumberNDA203696
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2013-07-01

NDC 0074-1052-10 [00074105210]

Lupaneta Pack KIT
Marketing CategoryNDA
Application NumberNDA203696
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-07-01

Drug Details

OpenFDA Data

SPL SET ID:f6709069-6a58-625b-d090-53a2c5cc6f3b
Manufacturer
RxNorm Concept Unique ID - RxCUI
  • 1488618
  • 1115457
  • 1115459
  • 1488619
  • 1000405
  • NDC Crossover Matching brand name "Lupaneta Pack" or generic name "Leuprolide Acetate And Norethindrone Acetate"

    NDCBrand NameGeneric Name
    0074-1052Lupaneta Packleuprolide acetate and norethindrone acetate
    0074-1053Lupaneta Packleuprolide acetate and norethindrone acetate

    Trademark Results [Lupaneta Pack]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    LUPANETA PACK
    LUPANETA PACK
    85758707 4564941 Live/Registered
    AbbVie Endocrine Inc.
    2012-10-19

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