NDC 36987-1430

Cauliflower

Cauliflower

Cauliflower 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 Cauliflower.

• Product ID: 36987-1430_dec580ea-73db-4658-9de1-440c19bb42b7
• NDC: 36987-1430
• Product Type: Human Prescription Drug
• Proprietary Name: Cauliflower
• Generic Name: Cauliflower
• Dosage Form: Injection, Solution
• Route of Administration: INTRADERMAL; SUBCUTANEOUS
• Marketing Start Date: 1972-08-29
• Marketing Category: BLA / BLA
• Application Number: BLA102192
• Labeler Name: Nelco Laboratories, Inc.
• Substance Name: CAULIFLOWER
• Active Ingredient Strength: 0 g/mL
• Pharm Classes: 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],Vegetable Proteins [CS]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 36987-1430-1

5 mL in 1 VIAL, MULTI-DOSE (36987-1430-1)

• Marketing Start Date: 1972-08-29
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 36987-1430-1 [36987143001]

Cauliflower INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102192
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1972-08-29
• Inactivation Date: 2019-10-21

NDC 36987-1430-3 [36987143003]

Cauliflower INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102192
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1972-08-29
• Inactivation Date: 2019-10-21

NDC 36987-1430-4 [36987143004]

Cauliflower INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102192
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1972-08-29
• Inactivation Date: 2019-10-21

NDC 36987-1430-2 [36987143002]

Cauliflower INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102192
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1972-08-29
• Inactivation Date: 2019-10-21

Drug Details

Active Ingredients

Ingredient	Strength
CAULIFLOWER	.05 g/mL

OpenFDA Data

• SPL SET ID: b65366b5-55ea-49dc-8011-8ef9af097291
• Manufacturer:
  • Nelco Laboratories, Inc.
• UNII:
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  • 9961HBA483
• RxNorm Concept Unique ID - RxCUI:
  • 891505
  • 895581
  • 901340
  • 900050
  • 895585
  • 891636
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  • 1011630
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  • 899909
  • 1011046
  • 901294
  • 1010929
  • 1011063
  • 899389
  • 899381
  • 1011069
  • 904651
  • 899385
  • 899632
  • 1000013
  • 899737
  • 904487
  • 899733
  • 1010858
  • 895573
  • 895577
  • 1010850
  • 1010918
  • 1010854
  • 1010856
  • 904649
  • 904642
  • 891671
  • 899640
  • 901320
  • 1011020
  • 899401
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  • 899483
  • 899880
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  • 966699
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  • 891679
  • 904533
  • 2103256
  • 891517
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  • 1006513
  • 895591
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  • 1011002
  • 899417
  • 899898
  • 899493
  • 899366
  • 892487
  • 899362
  • 1010700
  • 1011415
  • 899882
  • 1010974

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]
• Vegetable Proteins [CS]

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

NDC	Brand Name	Generic Name
22840-5713	Cauliflower	Brassica oleracea var. botrytis
36987-1430	Cauliflower	Cauliflower
36987-1431	Cauliflower	Cauliflower
36987-1432	Cauliflower	Cauliflower
36987-1433	Cauliflower	Cauliflower
49288-0107	Cauliflower	Cauliflower
54575-366	CAULIFLOWER	cauliflower