NDC 36987-2238

Tobacco Leaf

Tobacco Leaf

Tobacco Leaf 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 Tobacco Leaf.

Product ID36987-2238_f70401b9-9617-41a7-a0c6-ded6f6efa9fa
NDC36987-2238
Product TypeHuman Prescription Drug
Proprietary NameTobacco Leaf
Generic NameTobacco Leaf
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1972-08-29
Marketing CategoryBLA / BLA
Application NumberBLA102192
Labeler NameNelco Laboratories, Inc.
Substance NameTOBACCO LEAF
Active Ingredient Strength10000 [PNU]/mL
Pharm ClassesNon-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [CS],Plant Proteins [CS]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 36987-2238-3

30 mL in 1 VIAL, MULTI-DOSE (36987-2238-3)
Marketing Start Date1972-08-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 36987-2238-1 [36987223801]

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

NDC 36987-2238-3 [36987223803]

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

NDC 36987-2238-4 [36987223804]

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

NDC 36987-2238-2 [36987223802]

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

Drug Details

Active Ingredients

IngredientStrength
TOBACCO LEAF10000 [PNU]/mL

OpenFDA Data

SPL SET ID:fb086079-a3f1-458e-8910-2e72c7eae87c
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 889596
  • 1014203
  • 901354
  • 904851

    • Pharmacological Class

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

    NDC Crossover Matching brand name "Tobacco Leaf" or generic name "Tobacco Leaf"

    NDCBrand NameGeneric Name
    36987-2238Tobacco LeafTobacco Leaf
    36987-2239Tobacco LeafTobacco Leaf
    36987-2240Tobacco LeafTobacco Leaf
    36987-2242Tobacco LeafTobacco Leaf
    36987-2244Tobacco LeafTobacco Leaf
    36987-2245Tobacco LeafTobacco Leaf
    49643-022Tobacco LeafTobacco Leaf
    58264-0322A-30TOBACCO LEAF
    64117-993Motion Sickness 1TOBACCO LEAF
    0220-4906TabacumTOBACCO LEAF
    0220-4907TabacumTOBACCO LEAF
    0220-4908TabacumTOBACCO LEAF
    0220-4909TabacumTOBACCO LEAF
    0220-4910TabacumTOBACCO LEAF
    0220-4911TabacumTOBACCO LEAF
    0220-4916TabacumTOBACCO LEAF
    68428-661TabacumTOBACCO LEAF

    Trademark Results [Tobacco Leaf]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    TOBACCO LEAF
    TOBACCO LEAF
    78194339 2779687 Live/Registered
    Mottahedeh & Company, Inc.
    2002-12-13
    TOBACCO LEAF
    TOBACCO LEAF
    78194329 2871455 Live/Registered
    Mottahedeh & Company, Inc.
    2002-12-13
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