Carp
Allergenic Extract
Approved
Approval ID
ed374a8c-81d6-4389-b77b-00e5517ada89
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 10, 2009
Manufacturers
FDA
Nelco Laboratories, Inc.
DUNS: 054980867
Products 10
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Salmon
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-1248
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Salmon
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 10, 2009
FDA Product Classification
INGREDIENTS (5)
ATLANTIC SALMONActive
Quantity: 0.1 g in 1 mL
Code: 7062I37LB3
Classification: ACTIB
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
Pike
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-1240
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Pike
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 10, 2009
FDA Product Classification
INGREDIENTS (5)
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
NORTHERN PIKEActive
Quantity: 0.1 g in 1 mL
Code: 5JKY494U4L
Classification: ACTIB
WATERInactive
Code: 059QF0KO0R
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
Trout
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-1272
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Trout
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 10, 2009
FDA Product Classification
INGREDIENTS (5)
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
TROUTActive
Quantity: 0.1 g in 1 mL
Code: 7TI7U5PF2U
Classification: ACTIB
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
Tuna Fish
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-1276
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Tuna Fish
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 10, 2009
FDA Product Classification
INGREDIENTS (5)
TUNAActive
Quantity: 0.1 g in 1 mL
Code: V2T3IHT3E2
Classification: ACTIB
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
Smelt
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-1264
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Smelt
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 10, 2009
FDA Product Classification
INGREDIENTS (5)
SMELTActive
Quantity: 0.1 g in 1 mL
Code: 9VVF5SCM9I
Classification: ACTIB
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
Sardine
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-1252
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Sardine
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 10, 2009
FDA Product Classification
INGREDIENTS (5)
EUROPEAN PILCHARDActive
Quantity: 0.1 g in 1 mL
Code: 76780GX08D
Classification: ACTIB
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
Scallop
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-1256
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Scallop
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 10, 2009
FDA Product Classification
INGREDIENTS (5)
SCALLOPActive
Quantity: 0.1 g in 1 mL
Code: D380C73WOU
Classification: ACTIB
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
Shrimp
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-1260
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Shrimp
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 10, 2009
FDA Product Classification
INGREDIENTS (5)
SHRIMPActive
Quantity: 0.1 g in 1 mL
Code: 1891LE191T
Classification: ACTIB
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
White Fish
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-1280
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
White Fish
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 10, 2009
FDA Product Classification
INGREDIENTS (5)
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
WHITE FISHActive
Quantity: 0.1 g in 1 mL
Code: IA4C8ND0DT
Classification: ACTIB
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
Sword Fish
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-1268
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Sword Fish
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 10, 2009
FDA Product Classification
INGREDIENTS (5)
SWORDFISHActive
Quantity: 0.1 g in 1 mL
Code: 01695YPV36
Classification: ACTIB
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT