NDC 36987-1732

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: 36987-1732_20425e8b-8db3-4a2b-813b-7e3e1bc1c4e6
• NDC: 36987-1732
• 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 36987-1732-1

5 mL in 1 VIAL, MULTI-DOSE (36987-1732-1)

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

NDC SPL Data Element Entries

NDC 36987-1732-4 [36987173204]

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 36987-1732-3 [36987173203]

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 36987-1732-1 [36987173201]

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 36987-1732-2 [36987173202]

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	.1 g/mL

OpenFDA Data

• SPL SET ID: 6deab9bd-7a81-45ed-8a1c-b833b59b70b8
• Manufacturer:
  • Nelco Laboratories, Inc.
• UNII:
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  • 9961HBA483
• RxNorm Concept Unique ID - RxCUI:
  • 892502
  • 904822
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  • 891663
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  • 966633
  • 904413
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  • 891675
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  • 892529
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  • 1010910
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  • 895579
  • 892520
  • 891681
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  • 904435
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  • 1011411
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  • 901298
  • 895594
  • 904636
  • 904423
  • 1012166
  • 1010702
  • 1010704
  • 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]
• 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