NDC 36987-1035

Goose Feathers

Goose Feathers

Goose Feathers 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 Anser Anser Feather.

• Product ID: 36987-1035_8f2b01b8-e712-4107-b824-e1f07faa2a41
• NDC: 36987-1035
• Product Type: Human Prescription Drug
• Proprietary Name: Goose Feathers
• Generic Name: Goose Feathers
• 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: ANSER ANSER FEATHER
• Active Ingredient Strength: 20000 [PNU]/mL
• Pharm Classes: Non-Standardized Feather Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Feathers [CS],Allergens [CS],Increased IgG Production [PE]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 36987-1035-1

5 mL in 1 VIAL, MULTI-DOSE (36987-1035-1)

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

NDC SPL Data Element Entries

NDC 36987-1035-1 [36987103501]

Goose Feathers 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 36987-1035-2 [36987103502]

Goose Feathers 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 36987-1035-3 [36987103503]

Goose Feathers 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 36987-1035-4 [36987103504]

Goose Feathers 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
ANSER ANSER FEATHER	20000 [PNU]/mL

OpenFDA Data

• SPL SET ID: 001dcaf3-5838-4fb0-a4b8-d65ae2eb009e
• Manufacturer:
  • Nelco Laboratories, Inc.
• UNII:
  • X2W7CLE97T
  • 88VZV9HGT4
  • Z91WAU43WC
  • 83B65P4796
  • 9WN2H714TG
  • 390AN9GB09
  • 3K873H631W
  • 1FCM16V0FV
  • 7J12CD6O9L
  • GM3H4U6QS8
  • 15XI414745
  • 3EM4VW6TQN
  • Y69HPD48AI
  • JLG9853E2P
• RxNorm Concept Unique ID - RxCUI:
  • 895193
  • 889656
  • 895308
  • 895480
  • 895079
  • 894778
  • 895069
  • 895277
  • 895298
  • 895288
  • 895470
  • 895050
  • 894928
  • 894958

Pharmacological Class

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

NDC Crossover Matching brand name "Goose Feathers" or generic name "Goose Feathers"

NDC	Brand Name	Generic Name
22840-1159	Goose Feathers	Anser anser
22840-1160	Goose Feathers	Anser anser
22840-5113	Goose Feathers	Anser anser
36987-1033	Goose Feathers	Goose Feathers
36987-1034	Goose Feathers	Goose Feathers
36987-1035	Goose Feathers	Goose Feathers
36987-1036	Goose Feathers	Goose Feathers
36987-1037	Goose Feathers	Goose Feathers
36987-1038	Goose Feathers	Goose Feathers
36987-1039	Goose Feathers	Goose Feathers
36987-1040	Goose Feathers	Goose Feathers
54575-295	GOOSE FEATHERS	anser anser feather