NDC 36987-1709

Mustard Seed

Mustard Seed

Mustard Seed 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 Mustard Seed.

• Product ID: 36987-1709_255e0c54-6613-460b-a91f-452fdfd0319d
• NDC: 36987-1709
• Product Type: Human Prescription Drug
• Proprietary Name: Mustard Seed
• Generic Name: Mustard Seed
• 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: MUSTARD SEED
• 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],Increased IgG Production [PE],Allergens [CS],Food Additives [CS],Dietary Proteins [CS],Plant Proteins [CS],Seed Storage Proteins [CS]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 36987-1709-2

10 mL in 1 VIAL, MULTI-DOSE (36987-1709-2)

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

NDC SPL Data Element Entries

NDC 36987-1709-4 [36987170904]

Mustard Seed 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 36987-1709-2 [36987170902]

Mustard Seed 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 36987-1709-1 [36987170901]

Mustard Seed 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 36987-1709-3 [36987170903]

Mustard Seed 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
MUSTARD SEED	.1 g/mL

OpenFDA Data

• SPL SET ID: 42a03973-e3db-49f2-9264-f76aa831c045
• Manufacturer:
  • Nelco Laboratories, Inc.
• UNII:
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• RxNorm Concept Unique ID - RxCUI:
  • 892502
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  • 966633
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  • 901298
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  • 1012193
  • 904423
  • 1012166
  • 1011411
  • 1011417
  • 1010706
  • 1010708
  • 1010970
  • 1010976

Pharmacological Class

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

NDC Crossover Matching brand name "Mustard Seed" or generic name "Mustard Seed"

NDC	Brand Name	Generic Name
0268-6181	MUSTARD SEED	Mustard Seed
36987-1706	Mustard Seed	Mustard Seed
36987-1707	Mustard Seed	Mustard Seed
36987-1708	Mustard Seed	Mustard Seed
36987-1709	Mustard Seed	Mustard Seed
49288-0306	Mustard Seed	Mustard Seed
54575-415	MUSTARD SEED	mustard seed