NDC 49288-0426

Cayenne Pepper

Cayenne Pepper

Cayenne Pepper is a Intradermal; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Antigen Laboratories, Inc.. The primary component is Chili Pepper.

Product ID49288-0426_80e3a713-b3c2-4981-9f01-d987196bc528
NDC49288-0426
Product TypeHuman Prescription Drug
Proprietary NameCayenne Pepper
Generic NameCayenne Pepper
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1974-03-23
Marketing CategoryBLA / BLA
Application NumberBLA102223
Labeler NameAntigen Laboratories, Inc.
Substance NameCHILI PEPPER
Active Ingredient Strength0 g/mL
Pharm ClassesNon-Standardized Plant Allergenic Extract [EPC],Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Plant Proteins [CS],Vegetable Proteins [CS]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 49288-0426-3

10 mL in 1 VIAL, MULTI-DOSE (49288-0426-3)
Marketing Start Date1974-03-23
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 49288-0426-3 [49288042603]

Cayenne Pepper INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102223
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1974-03-23
Inactivation Date2019-10-21

NDC 49288-0426-2 [49288042602]

Cayenne Pepper INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102223
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1974-03-23
Inactivation Date2019-10-21

NDC 49288-0426-5 [49288042605]

Cayenne Pepper INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102223
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1974-03-23
Inactivation Date2019-10-21

NDC 49288-0426-1 [49288042601]

Cayenne Pepper INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102223
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1974-03-23
Inactivation Date2019-10-21

NDC 49288-0426-4 [49288042604]

Cayenne Pepper INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102223
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1974-03-23
Inactivation Date2019-10-21

Drug Details

Active Ingredients

IngredientStrength
CHILI PEPPER.05 g/mL

OpenFDA Data

SPL SET ID:addbb916-198c-4992-98c3-a66b19a1e241
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1014714
  • 1006343
  • 904501
  • 967981
  • 966699
  • Pharmacological Class

    • Non-Standardized Plant Allergenic Extract [EPC]
    • Non-Standardized Food Allergenic Extract [EPC]
    • Increased Histamine Release [PE]
    • Cell-mediated Immunity [PE]
    • Allergens [CS]
    • Dietary Proteins [CS]
    • Plant Proteins [CS]
    • Vegetable Proteins [CS]

    NDC Crossover Matching brand name "Cayenne Pepper" or generic name "Cayenne Pepper"

    NDCBrand NameGeneric Name
    49288-0426Cayenne PepperCayenne Pepper
    62106-7576CAPSICUM ANNUUMCayenne pepper

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