NDC 36987-1731

Poppyseed

Poppyseed

Poppyseed 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 Poppy Seed.

• Product ID: 36987-1731_c9d2ad91-0541-4504-a528-c0cc93a99e4e
• NDC: 36987-1731
• Product Type: Human Prescription Drug
• Proprietary Name: Poppyseed
• Generic Name: Poppyseed
• 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: POPPY 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],Allergens [CS],Dietary Proteins [CS],Plant Proteins [CS],Seed Storage Proteins [CS]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 36987-1731-1

5 mL in 1 VIAL, MULTI-DOSE (36987-1731-1)

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

NDC SPL Data Element Entries

NDC 36987-1731-3 [36987173103]

Poppyseed 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 36987-1731-2 [36987173102]

Poppyseed 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 36987-1731-4 [36987173104]

Poppyseed 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 36987-1731-1 [36987173101]

Poppyseed 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
POPPY SEED	.05 g/mL

OpenFDA Data

• SPL SET ID: 9cf0d617-467d-461f-b6d3-d2d926982bb7
• Manufacturer:
  • Nelco Laboratories, Inc.
• UNII:
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  • 9961HBA483
• RxNorm Concept Unique ID - RxCUI:
  • 891505
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  • 1011069
  • 904651
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  • 899632
  • 1000013
  • 899737
  • 904487
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  • 891671
  • 899640
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  • 904533
  • 2103256
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  • 899417
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  • 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]
• Seed Storage Proteins [CS]

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

NDC	Brand Name	Generic Name
36987-1730	Poppyseed	Poppyseed
36987-1731	Poppyseed	Poppyseed
36987-1732	Poppyseed	Poppyseed
36987-1733	Poppyseed	Poppyseed