NDC 49288-0071

Bay Leaf

Bay Leaf

Bay Leaf 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 Laurus Nobilis.

Product ID49288-0071_1d11d7ba-8b48-401c-a02e-42b54abb4296
NDC49288-0071
Product TypeHuman Prescription Drug
Proprietary NameBay Leaf
Generic NameBay Leaf
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1974-03-23
Marketing CategoryBLA / BLA
Application NumberBLA102223
Labeler NameAntigen Laboratories, Inc.
Substance NameLAURUS NOBILIS
Active Ingredient Strength0 g/mL
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 49288-0071-5

50 mL in 1 VIAL, MULTI-DOSE (49288-0071-5)
Marketing Start Date1974-03-23
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 49288-0071-2 [49288007102]

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

NDC 49288-0071-5 [49288007105]

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

NDC 49288-0071-3 [49288007103]

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

NDC 49288-0071-4 [49288007104]

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

NDC 49288-0071-1 [49288007101]

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

Drug Details

Active Ingredients

IngredientStrength
LAURUS NOBILIS.05 g/mL

OpenFDA Data

SPL SET ID:f2adabd1-ea12-437a-a902-da240cf2a62c
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 901340
  • 900050
  • 895585
  • 891636
  • 899664
  • 1011630
  • 967977
  • 899352
  • 899354
  • 899469
  • 899358
  • 1010882
  • 978960
  • 905501
  • 899773
  • 899672
  • 899676
  • 901372
  • 899479
  • 899475
  • 899473
  • 899876
  • 904479
  • 891724
  • 901368
  • 891640
  • 891644
  • 899447
  • 902747
  • 891799
  • 899455
  • 899451
  • 891650
  • 899757
  • 891655
  • 899459
  • 1006513
  • 901316
  • 967985
  • 901310
  • 891661
  • 899397
  • 899393
  • 899423
  • 899427
  • 899741
  • 899745
  • 904868
  • 901306
  • 899909
  • 901349
  • 901294
  • 899493
  • 899389
  • 904487
  • 904651
  • 899385
  • 899632
  • 1000013
  • 899737
  • 901332
  • 899733
  • 895573
  • 904649
  • 904642
  • 891671
  • 899640
  • 901320
  • 899401
  • 901206
  • 901202
  • 899483
  • 899880
  • 899727
  • 899886
  • 891679
  • 899381
  • 904533
  • 2103256
  • 891698
  • 891517
  • 891690
  • 892320
  • 891614
  • 899655
  • 899417
  • 899898
  • 901198
  • 899366
  • 899362
  • 901194
  • 899882
  • NDC Crossover Matching brand name "Bay Leaf" or generic name "Bay Leaf"

    NDCBrand NameGeneric Name
    36987-1666Bay LeafBay Leaf
    36987-1667Bay LeafBay Leaf
    36987-1668Bay LeafBay Leaf
    36987-1669Bay LeafBay Leaf
    49288-0071Bay LeafBay Leaf

    Trademark Results [Bay Leaf]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    BAY LEAF
    BAY LEAF
    86863359 not registered Dead/Abandoned
    ARORA KAMAL
    2015-12-31
    BAY LEAF
    BAY LEAF
    85819569 4641766 Live/Registered
    FIOR DI SOLE, LLC
    2013-01-09

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