NDC 49288-0120

Coconut

Coconut

Coconut 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 Coconut.

• Product ID: 49288-0120_1d11d7ba-8b48-401c-a02e-42b54abb4296
• NDC: 49288-0120
• Product Type: Human Prescription Drug
• Proprietary Name: Coconut
• Generic Name: Coconut
• Dosage Form: Injection, Solution
• Route of Administration: INTRADERMAL; SUBCUTANEOUS
• Marketing Start Date: 1974-03-23
• Marketing Category: BLA / BLA
• Application Number: BLA102223
• Labeler Name: Antigen Laboratories, Inc.
• Substance Name: COCONUT
• Active Ingredient Strength: 0 g/mL
• Pharm Classes: Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Fruit Proteins [EXT]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 49288-0120-3

10 mL in 1 VIAL, MULTI-DOSE (49288-0120-3)

• Marketing Start Date: 1974-03-23
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 49288-0120-2 [49288012002]

Coconut INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102223
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1974-03-23
• Inactivation Date: 2019-10-21

NDC 49288-0120-4 [49288012004]

Coconut INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102223
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1974-03-23
• Inactivation Date: 2019-10-21

NDC 49288-0120-3 [49288012003]

Coconut INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102223
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1974-03-23
• Inactivation Date: 2019-10-21

NDC 49288-0120-1 [49288012001]

Coconut INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102223
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1974-03-23
• Inactivation Date: 2019-10-21

NDC 49288-0120-5 [49288012005]

Coconut INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102223
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1974-03-23
• Inactivation Date: 2019-10-21

Drug Details

Active Ingredients

Ingredient	Strength
COCONUT	.05 g/mL

OpenFDA Data

• SPL SET ID: f2adabd1-ea12-437a-a902-da240cf2a62c
• Manufacturer:
  • Antigen Laboratories, Inc.
• UNII:
  • N487KM8COK
  • 93T4562ZI3
  • AEE24M3MQ9
  • GW0W1Y9I97
  • 3RT3536DHY
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• RxNorm Concept Unique ID - RxCUI:
  • 901340
  • 900050
  • 895585
  • 891636
  • 899664
  • 1011630
  • 967977
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  • 904479
  • 891724
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  • 899397
  • 899393
  • 899423
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  • 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

Pharmacological Class

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

NDC Crossover Matching brand name "Coconut" or generic name "Coconut"

NDC	Brand Name	Generic Name
0268-6127	COCONUT	COCONUT
22840-5784	Coconut	Cocos nucifera
36987-1538	Coconut	Coconut
36987-1539	Coconut	Coconut
36987-1540	Coconut	Coconut
36987-1541	Coconut	Coconut
49288-0120	Coconut	Coconut
54575-378	COCONUT	coconut