NDC 49288-0401

Queen Palm

Queen Palm

Queen Palm 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 Syagrus Romanzoffiana Pollen.

• Product ID: 49288-0401_13c9eea1-38b5-472b-b735-a814ca886718
• NDC: 49288-0401
• Product Type: Human Prescription Drug
• Proprietary Name: Queen Palm
• Generic Name: Queen Palm
• 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: SYAGRUS ROMANZOFFIANA POLLEN
• Active Ingredient Strength: 0 g/mL
• Pharm Classes: Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 49288-0401-5

50 mL in 1 VIAL, MULTI-DOSE (49288-0401-5)

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

NDC SPL Data Element Entries

NDC 49288-0401-5 [49288040105]

Queen Palm 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 49288-0401-3 [49288040103]

Queen Palm 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 49288-0401-2 [49288040102]

Queen Palm 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 49288-0401-1 [49288040101]

Queen Palm 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 49288-0401-4 [49288040104]

Queen Palm 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
SYAGRUS ROMANZOFFIANA POLLEN	.05 g/mL

OpenFDA Data

• SPL SET ID: 3be2afc4-b2dc-4b0f-b314-5ade25922b66
• Manufacturer:
  • Antigen Laboratories, Inc.
• UNII:
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  • 43R41XZ627
  • KPO1Z9N98A
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• RxNorm Concept Unique ID - RxCUI:
  • 852327
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  • 867300
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  • 900102
  • 900540
  • 900990
  • 852385
  • 852147
  • 852143

Pharmacological Class

• Non-Standardized Pollen Allergenic Extract [EPC]
• Increased Histamine Release [PE]
• Cell-mediated Immunity [PE]
• Increased IgG Production [PE]
• Pollen [CS]
• Allergens [CS]

NDC Crossover Matching brand name "Queen Palm" or generic name "Queen Palm"

NDC	Brand Name	Generic Name
36987-2917	Queen Palm	Queen Palm
36987-2918	Queen Palm	Queen Palm
36987-2919	Queen Palm	Queen Palm
36987-2920	Queen Palm	Queen Palm
36987-2921	Queen Palm	Queen Palm
36987-2922	Queen Palm	Queen Palm
36987-2923	Queen Palm	Queen Palm
36987-2924	Queen Palm	Queen Palm
49288-0401	Queen Palm	Queen Palm