NDC 36987-2393

Salt Grass

Salt Grass

Salt Grass 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 Distichlis Spicata Pollen.

Product ID36987-2393_467064a9-eca5-4b65-bdbb-0323fb27bcf6
NDC36987-2393
Product TypeHuman Prescription Drug
Proprietary NameSalt Grass
Generic NameSalt Grass
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1972-08-29
Marketing CategoryBLA / BLA
Application NumberBLA102192
Labeler NameNelco Laboratories, Inc.
Substance NameDISTICHLIS SPICATA 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 36987-2393-1

5 mL in 1 VIAL, MULTI-DOSE (36987-2393-1)
Marketing Start Date1972-08-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 36987-2393-1 [36987239301]

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

NDC 36987-2393-3 [36987239303]

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

NDC 36987-2393-2 [36987239302]

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

NDC 36987-2393-4 [36987239304]

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

Drug Details

Active Ingredients

IngredientStrength
DISTICHLIS SPICATA POLLEN20000 [PNU]/mL

OpenFDA Data

SPL SET ID:394c5437-08b9-49ae-a90c-2c5d5b449344
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 889666
  • 897359
  • 899541
  • 889565
  • 900012
  • 897351
  • 898409
  • 1014347
  • 899976
  • 900161
  • 898136
  • 1044242
  • 1013966
  • 889530
  • 1044526
  • 1044504
  • 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 "Salt Grass" or generic name "Salt Grass"

    NDCBrand NameGeneric Name
    36987-2391Salt GrassSalt Grass
    36987-2392Salt GrassSalt Grass
    36987-2393Salt GrassSalt Grass
    36987-2394Salt GrassSalt Grass
    36987-2395Salt GrassSalt Grass
    36987-2396Salt GrassSalt Grass
    36987-2397Salt GrassSalt Grass
    36987-2398Salt GrassSalt Grass
    0268-1476DISTICHLIS SPICATA POLLENSalt Grass
    0268-1477DISTICHLIS SPICATA POLLENSalt Grass
    0268-6757DISTICHLIS SPICATA POLLENSalt Grass

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