NDC 36987-2202

Cotton Linters

Cotton Linters

Cotton Linters 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 Cotton Fiber.

Product ID36987-2202_ec73bb3c-d08d-4a3b-92a9-d2bfd09da169
NDC36987-2202
Product TypeHuman Prescription Drug
Proprietary NameCotton Linters
Generic NameCotton Linters
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1972-08-29
Marketing CategoryBLA / BLA
Application NumberBLA102192
Labeler NameNelco Laboratories, Inc.
Substance NameCOTTON FIBER
Active Ingredient Strength0 g/mL
Pharm ClassesNon-Standardized Plant Fiber Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Plant Proteins [CS],Allergens [CS]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 36987-2202-4

50 mL in 1 VIAL, MULTI-DOSE (36987-2202-4)
Marketing Start Date1972-08-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 36987-2202-4 [36987220204]

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

NDC 36987-2202-2 [36987220202]

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

NDC 36987-2202-3 [36987220203]

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

NDC 36987-2202-1 [36987220201]

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

Drug Details

Active Ingredients

IngredientStrength
COTTON FIBER.05 g/mL

OpenFDA Data

SPL SET ID:0fb71326-54c9-4139-befe-06ca832d02c8
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 904846
  • 889598
  • 966928
  • 1098356
  • 904681
  • 966958
  • 978958
  • 904965
  • 1014199
  • Pharmacological Class

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

    NDC Crossover Matching brand name "Cotton Linters" or generic name "Cotton Linters"

    NDCBrand NameGeneric Name
    22840-1519Cotton LintersGossypium hirsutum
    22840-1520Cotton LintersGossypium hirsutum
    22840-1553Cotton LintersGossypium hirsutum
    22840-5508Cotton LintersGossypium hirsutum
    36987-2202Cotton LintersCotton Linters
    36987-2203Cotton LintersCotton Linters
    36987-2204Cotton LintersCotton Linters
    36987-2205Cotton LintersCotton Linters
    49288-0154Cotton LintersCotton Linters
    49643-004Cotton LintersCotton Linters
    54575-284COTTON LINTERScotton fiber
    0268-0609COTTON FIBERCOTTON LINTERS
    0268-6303COTTON FIBERCotton Linters

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