MedPath

Aspergillus fumigatus

Allergenic Extract

Approved
Approval ID

3484572a-db45-479f-8ba4-39a9d1b00d04

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Dec 14, 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.

Oat Smut

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code36987-2161
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Oat Smut
Product Specifications
Route of AdministrationSUBCUTANEOUS, INTRADERMAL
Effective DateDecember 14, 2009
FDA Product Classification

INGREDIENTS (5)

PHENOLInactive
Code: 339NCG44TV
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
USTILAGO AVENAEActive
Quantity: 0.1 g in 1 mL
Code: YIH315U1TU
Classification: ACTIB
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT

Corn Smut

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code36987-2152
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Corn Smut
Product Specifications
Route of AdministrationSUBCUTANEOUS, INTRADERMAL
Effective DateDecember 14, 2009
FDA Product Classification

INGREDIENTS (5)

USTILAGO MAYDISActive
Quantity: 0.1 g in 1 mL
Code: 4K7Z7K7SWG
Classification: ACTIB
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT

Curvularia inequalis

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code36987-1963
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Curvularia inequalis
Product Specifications
Route of AdministrationSUBCUTANEOUS, INTRADERMAL
Effective DateDecember 14, 2009
FDA Product Classification

INGREDIENTS (5)

CURVULARIA INAEQUALISActive
Quantity: 0.1 g in 1 mL
Code: W042YAB8JC
Classification: ACTIB
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT

Wheat Bunt

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code36987-2179
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Wheat Bunt
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 14, 2009
FDA Product Classification

INGREDIENTS (5)

TILLETIA CARIESActive
Quantity: 0.1 g in 1 mL
Code: C7000B9PQI
Classification: ACTIB
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT

Trichoderma harzianam

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code36987-2125
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Trichoderma harzianam
Product Specifications
Route of AdministrationSUBCUTANEOUS, INTRADERMAL
Effective DateDecember 14, 2009
FDA Product Classification

INGREDIENTS (5)

SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
TRICHODERMA HARZIANUMActive
Quantity: 0.1 g in 1 mL
Code: CA33Q4013Q
Classification: ACTIB

Fusarium compactum

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code36987-1981
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Fusarium compactum
Product Specifications
Route of AdministrationSUBCUTANEOUS, INTRADERMAL
Effective DateDecember 14, 2009
FDA Product Classification

INGREDIENTS (5)

PHENOLInactive
Code: 339NCG44TV
Classification: IACT
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
FUSARIUM COMPACTUMActive
Quantity: 0.1 g in 1 mL
Code: V4OQR60A5P
Classification: ACTIB
WATERInactive
Code: 059QF0KO0R
Classification: IACT

Wheat Stem Rust

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code36987-2188
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Wheat Stem Rust
Product Specifications
Route of AdministrationSUBCUTANEOUS, INTRADERMAL
Effective DateDecember 14, 2009
FDA Product Classification

INGREDIENTS (5)

WATERInactive
Code: 059QF0KO0R
Classification: IACT
PUCCINIA GRAMINISActive
Quantity: 0.1 g in 1 mL
Code: O0HJ02QBWN
Classification: ACTIB
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT

Trichophyton mentagrophytes

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code36987-2134
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Trichophyton mentagrophytes
Product Specifications
Route of AdministrationSUBCUTANEOUS, INTRADERMAL
Effective DateDecember 14, 2009
FDA Product Classification

INGREDIENTS (5)

TRICHOPHYTON MENTAGROPHYTESActive
Quantity: 0.1 g in 1 mL
Code: 199I7J3JIV
Classification: ACTIB
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT

Wheat Smut

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code36987-2170
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Wheat Smut
Product Specifications
Route of AdministrationSUBCUTANEOUS, INTRADERMAL
Effective DateDecember 14, 2009
FDA Product Classification

INGREDIENTS (5)

USTILAGO TRITICIActive
Quantity: 0.1 g in 1 mL
Code: BV82OL2IZ8
Classification: ACTIB
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT

Phoma glomerata

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code36987-2062
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Phoma glomerata
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 14, 2009
FDA Product Classification

INGREDIENTS (5)

PHOMA GLOMERATAActive
Quantity: 0.1 g in 1 mL
Code: UPX000VMIF
Classification: ACTIB
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT

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