NDC 49288-0567

Tea

Tea

Tea 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 Tea Leaf.

Product ID49288-0567_80e3a713-b3c2-4981-9f01-d987196bc528
NDC49288-0567
Product TypeHuman Prescription Drug
Proprietary NameTea
Generic NameTea
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1974-03-23
Marketing CategoryBLA / BLA
Application NumberBLA102223
Labeler NameAntigen Laboratories, Inc.
Substance NameTEA LEAF
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]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 49288-0567-4

30 mL in 1 VIAL, MULTI-DOSE (49288-0567-4)
Marketing Start Date1974-03-23
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 49288-0567-1 [49288056701]

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

NDC 49288-0567-4 [49288056704]

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

NDC 49288-0567-5 [49288056705]

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

NDC 49288-0567-3 [49288056703]

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

NDC 49288-0567-2 [49288056702]

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

Drug Details

Active Ingredients

IngredientStrength
TEA LEAF.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]

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