NDC 36987-1028

Duck Feathers

Duck Feathers

Duck 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 Anas Platyrhynchos Feather.

• Product ID: 36987-1028_b8207809-3a22-4e67-8783-87f426677ccf
• NDC: 36987-1028
• Product Type: Human Prescription Drug
• Proprietary Name: Duck Feathers
• Generic Name: Duck 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: ANAS PLATYRHYNCHOS 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 36987-1028-3

30 mL in 1 VIAL, MULTI-DOSE (36987-1028-3)

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

NDC SPL Data Element Entries

NDC 36987-1028-3 [36987102803]

Duck 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 36987-1028-1 [36987102801]

Duck 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 36987-1028-4 [36987102804]

Duck 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 36987-1028-2 [36987102802]

Duck 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
ANAS PLATYRHYNCHOS FEATHER	20000 [PNU]/mL

OpenFDA Data

• SPL SET ID: d4a4a463-98b3-4264-b6c9-0fb0c2edd2a7
• 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 "Duck Feathers" or generic name "Duck Feathers"

NDC	Brand Name	Generic Name
22840-1157	Duck Feathers	Anas platyrhynchos
22840-1176	Duck Feathers	Anas platyrhynchos
22840-5112	Duck Feathers	Anas platyrhynchos
36987-1025	Duck Feathers	Duck Feathers
36987-1026	Duck Feathers	Duck Feathers
36987-1027	Duck Feathers	Duck Feathers
36987-1028	Duck Feathers	Duck Feathers
36987-1029	Duck Feathers	Duck Feathers
36987-1030	Duck Feathers	Duck Feathers
36987-1031	Duck Feathers	Duck Feathers
36987-1032	Duck Feathers	Duck Feathers
54575-294	DUCK FEATHERS	anas platyrhynchos feather