NDC 0002-8149

HUMATROPE

Somatropin

HUMATROPE is a Intramuscular; Subcutaneous Kit in the Human Prescription Drug category. It is labeled and distributed by Eli Lilly And Company. The primary component is .

Product ID0002-8149_0ed9ddb4-0667-439a-8c1c-8f56d9b011b2
NDC0002-8149
Product TypeHuman Prescription Drug
Proprietary NameHUMATROPE
Generic NameSomatropin
Dosage FormKit
Route of AdministrationINTRAMUSCULAR; SUBCUTANEOUS
Marketing Start Date2006-01-27
Marketing CategoryBLA / NDA
Application NumberBLA019640
Labeler NameEli Lilly and Company
Active Ingredient Strength0
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 0002-8149-01

1 TRAY in 1 CARTON (0002-8149-01) > 1 KIT in 1 TRAY * 2.88 mL in 1 CARTRIDGE (0002-7556-01) * 2.88 mL in 1 SYRINGE (0002-7619-01)
Marketing Start Date2006-01-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0002-8149-01 [00002814901]

HUMATROPE KIT
Marketing CategoryNDA
Application NumberNDA019640
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-01-27

Drug Details

OpenFDA Data

SPL SET ID:a774e1ae-3997-49ee-8b0e-99a2b315d409
Manufacturer
RxNorm Concept Unique ID - RxCUI
  • 582969
  • 729232
  • 582974
  • 582971
  • 207834
  • 729234
  • 346494
  • 582976
  • UPC Code
  • 0300028149010
  • 0300028147016
  • 0300027335117
  • NDC Crossover Matching brand name "HUMATROPE" or generic name "Somatropin"

    NDCBrand NameGeneric Name
    0002-7335HUMATROPESomatropin
    0002-8147HUMATROPESomatropin
    0002-8148HUMATROPESomatropin
    0002-8149HUMATROPESomatropin
    0013-2626GENOTROPINsomatropin
    0013-2646GENOTROPINsomatropin
    0013-2649GENOTROPINsomatropin
    0013-2650GENOTROPINsomatropin
    0013-2651GENOTROPINsomatropin

    Trademark Results [HUMATROPE]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    HUMATROPE
    HUMATROPE
    73593339 1415565 Live/Registered
    ELI LILLY AND COMPANY
    1986-04-14

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