NDC 49288-0188

Egg White

Egg White

Egg White 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 Egg White.

Product ID49288-0188_ab729e90-03ec-4b3a-8c11-390b49ff5173
NDC49288-0188
Product TypeHuman Prescription Drug
Proprietary NameEgg White
Generic NameEgg White
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1974-03-23
Marketing CategoryBLA / BLA
Application NumberBLA102223
Labeler NameAntigen Laboratories, Inc.
Substance NameEGG WHITE
Active Ingredient Strength0 g/mL
Pharm ClassesCell-mediated Immunity [PE],Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Allergens [CS],Egg Proteins, Dietary [CS],Dietary Proteins [CS]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 49288-0188-2

5 mL in 1 VIAL, MULTI-DOSE (49288-0188-2)
Marketing Start Date1974-03-23
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 49288-0188-5 [49288018805]

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

NDC 49288-0188-4 [49288018804]

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

NDC 49288-0188-1 [49288018801]

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

NDC 49288-0188-3 [49288018803]

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

NDC 49288-0188-2 [49288018802]

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

Drug Details

Active Ingredients

IngredientStrength
EGG WHITE.05 g/mL

OpenFDA Data

SPL SET ID:422e7c71-ab7d-4064-97b9-a2d0527f18b0
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 892668
  • 905493
  • 966672
  • 904657
  • 966654
  • 899626
  • 967004
  • 966934
  • 892619
  • 1006349
  • 966942
  • 966649
  • 905333
  • Pharmacological Class

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

    NDC Crossover Matching brand name "Egg White" or generic name "Egg White"

    NDCBrand NameGeneric Name
    0268-6133EGG WHITEEGG WHITE
    36987-1130Egg WhiteEgg White
    36987-1131Egg WhiteEgg White
    36987-1132Egg WhiteEgg White
    36987-1133Egg WhiteEgg White
    49288-0188Egg WhiteEgg White
    54575-389EGG WHITEegg white

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