NDC 36987-2618

Arizona Cypress

Arizona Cypress

Arizona Cypress 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 Cupressus Arizonica Pollen.

Product ID36987-2618_ca9dfb3b-60b5-4a0b-83ff-990c5959c205
NDC36987-2618
Product TypeHuman Prescription Drug
Proprietary NameArizona Cypress
Generic NameArizona Cypress
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1972-08-29
Marketing CategoryBLA / BLA
Application NumberBLA102192
Labeler NameNelco Laboratories, Inc.
Substance NameCUPRESSUS ARIZONICA POLLEN
Active Ingredient Strength0 g/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 36987-2618-2

10 mL in 1 VIAL, MULTI-DOSE (36987-2618-2)
Marketing Start Date1972-08-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 36987-2618-1 [36987261801]

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

NDC 36987-2618-3 [36987261803]

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

NDC 36987-2618-2 [36987261802]

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

NDC 36987-2618-4 [36987261804]

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

Drug Details

Active Ingredients

IngredientStrength
CUPRESSUS ARIZONICA POLLEN.05 g/mL

OpenFDA Data

SPL SET ID:40e787f4-4eef-40de-be33-86ab7b36f0f3
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 852672
  • 851905
  • 852753
  • 852572
  • 851913
  • 851869
  • 900734
  • 852656
  • 851739
  • 851917
  • 1006374
  • 900994
  • 900048
  • 1044349
  • 852181
  • 1111027
  • 852741
  • 852342
  • 852263
  • 852453
  • 852712
  • 895356
  • 852612
  • 852224
  • 852630
  • 852305
  • 889650
  • 900773
  • 852600
  • 900116
  • 1014363
  • 852323
  • 1115265
  • 852817
  • 852422
  • 852173
  • 852284
  • 903916
  • 901025
  • 852177
  • 897406
  • 852151
  • 852297
  • 1013964
  • 1013916
  • 851747
  • 852366
  • 852604
  • 851743
  • 1299985
  • 852499
  • 852057
  • 851877
  • 852385
  • 899596
  • 852719
  • 852584
  • 1014194
  • 1044329
  • 852275
  • 852351
  • 852379
  • 852271
  • 852232
  • 852196
  • 852564
  • 995757
  • 852358
  • 852279
  • 852809
  • 852370
  • 900111
  • 852592
  • 900746
  • 852683
  • 867300
  • 898012
  • 852749
  • 852165
  • 852580
  • 852147
  • 852625
  • 901018
  • 852143
  • 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 "Arizona Cypress" or generic name "Arizona Cypress"

    NDCBrand NameGeneric Name
    36987-2613Arizona CypressArizona Cypress
    36987-2614Arizona CypressArizona Cypress
    36987-2615Arizona CypressArizona Cypress
    36987-2616Arizona CypressArizona Cypress
    36987-2617Arizona CypressArizona Cypress
    36987-2618Arizona CypressArizona Cypress
    36987-2619Arizona CypressArizona Cypress
    36987-2620Arizona CypressArizona Cypress
    49288-0136Arizona CypressArizona Cypress
    0268-6619CUPRESSUS ARIZONICA POLLENArizona Cypress
    0268-6703CUPRESSUS ARIZONICA POLLENArizona Cypress

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