NDC 36987-3376

Greasewood

Greasewood

Greasewood is a Intradermal; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Nelco Laboratories, Inc.. The primary component is Sarcobatus Vermiculatus Pollen.

Product ID36987-3376_9e270517-2bc2-4a64-878b-972dfe8eb086
NDC36987-3376
Product TypeHuman Prescription Drug
Proprietary NameGreasewood
Generic NameGreasewood
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1972-08-29
Marketing CategoryBLA / BLA
Application NumberBLA102192
Labeler NameNelco Laboratories, Inc.
Substance NameSARCOBATUS VERMICULATUS POLLEN
Active Ingredient Strength20000 [PNU]/mL
Pharm ClassesNon-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 36987-3376-4

50 mL in 1 VIAL, MULTI-DOSE (36987-3376-4)
Marketing Start Date1972-08-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 36987-3376-1 [36987337601]

Greasewood INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102192
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1972-08-29
Inactivation Date2019-10-21

NDC 36987-3376-4 [36987337604]

Greasewood INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102192
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1972-08-29
Inactivation Date2019-10-21

NDC 36987-3376-2 [36987337602]

Greasewood INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102192
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1972-08-29
Inactivation Date2019-10-21

NDC 36987-3376-3 [36987337603]

Greasewood INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102192
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1972-08-29
Inactivation Date2019-10-21

Drug Details

Active Ingredients

IngredientStrength
SARCOBATUS VERMICULATUS POLLEN20000 [PNU]/mL

OpenFDA Data

SPL SET ID:7f312e04-f414-4f1e-bce2-ea43fe3d93f9
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 896125
  • 897966
  • 897313
  • 896288
  • 1006365
  • 895677
  • 1006486
  • 895612
  • 895912
  • 896208
  • 897374
  • 896088
  • 896263
  • 1013972
  • 1013970
  • 897400
  • 897995
  • 897975
  • 897957
  • 896171
  • 901475
  • 896298
  • 901493
  • 1006357
  • 896156
  • 897325
  • 896078
  • 895725
  • 1006492
  • 897341
  • 896255
  • 896196
  • 897512
  • 897382
  • 898337
  • 897949
  • 896279
  • Pharmacological Class

    • Non-Standardized Pollen Allergenic Extract [EPC]
    • Increased Histamine Release [PE]
    • Cell-mediated Immunity [PE]
    • Increased IgG Production [PE]
    • Pollen [CS]
    • Allergens [CS]

    NDC Crossover Matching brand name "Greasewood" or generic name "Greasewood"

    NDCBrand NameGeneric Name
    36987-3373GreasewoodGreasewood
    36987-3374GreasewoodGreasewood
    36987-3375GreasewoodGreasewood
    36987-3376GreasewoodGreasewood
    36987-3377GreasewoodGreasewood
    36987-3378GreasewoodGreasewood
    36987-3379GreasewoodGreasewood
    36987-3380GreasewoodGreasewood

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