NDC 36987-1813

Mosquito

Mosquito

Mosquito 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 Aedes Taeniorhynchus.

• Product ID: 36987-1813_f243b580-e924-4bc5-9214-b3dfdf50a0a5
• NDC: 36987-1813
• Product Type: Human Prescription Drug
• Proprietary Name: Mosquito
• Generic Name: Mosquito
• 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: AEDES TAENIORHYNCHUS
• Active Ingredient Strength: 10000 [PNU]/mL
• Pharm Classes: Non-Standardized Insect Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Insect Proteins [CS],Allergens [CS]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 36987-1813-3

30 mL in 1 VIAL, MULTI-DOSE (36987-1813-3)

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

NDC SPL Data Element Entries

NDC 36987-1813-4 [36987181304]

Mosquito 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 36987-1813-2 [36987181302]

Mosquito 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 36987-1813-1 [36987181301]

Mosquito 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 36987-1813-3 [36987181303]

Mosquito 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
AEDES TAENIORHYNCHUS	10000 [PNU]/mL

OpenFDA Data

• SPL SET ID: 470d7a58-b8ee-4f97-a5e2-3e8c65096231
• Manufacturer:
  • Nelco Laboratories, Inc.
• UNII:
  • 5O7CR4P444
  • PV7823W303
  • BN2DNW66IQ
• RxNorm Concept Unique ID - RxCUI:
  • 967928
  • 968015
  • 905111
  • 905264
  • 905290

Pharmacological Class

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

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

NDC	Brand Name	Generic Name
0268-0725	MOSQUITO	CULEX PIPIENS
22840-1022	Mosquito	Aedes taeniorhynchus
22840-1029	Mosquito	Aedes taeniorhynchus
22840-1030	Mosquito	Aedes taeniorhynchus
22840-5009	Mosquito	Aedes taeniorhynchus
36987-1812	Mosquito	Mosquito
36987-1813	Mosquito	Mosquito
36987-1814	Mosquito	Mosquito
36987-1815	Mosquito	Mosquito
36987-1816	Mosquito	Mosquito
36987-1817	Mosquito	Mosquito
36987-1818	Mosquito	Mosquito
36987-1819	Mosquito	Mosquito