Trichophyton for Intradermal Skin Testing
ALLERGENIC EXTRACT for Intradermal Skin Testing
Approved
Approval ID
aaeffe62-b538-43ca-a3b9-47e28b765d89
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
May 13, 2009
Manufacturers
FDA
Allermed Laboratories, Inc.
DUNS: 073364531
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Trichophyton mentagrophytes and Trichophyton rubrum
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code49643-128
Application NumberBLA102211
Product Classification
M
Marketing Category
C73585
G
Generic Name
Trichophyton mentagrophytes and Trichophyton rubrum
Product Specifications
Route of AdministrationCUTANEOUS, SUBCUTANEOUS, INTRADERMAL
Effective DateMarch 19, 2009
FDA Product Classification
INGREDIENTS (7)
Trichophyton rubrumActive
Quantity: 1 g in 1000 mL
Code: 2ZAU32517N
Classification: ACTIB
Trichophyton mentagrophytesActive
Quantity: 1 g in 1000 mL
Code: 199I7J3JIV
Classification: ACTIB
Sodium chlorideInactive
Quantity: 0.25 g in 100 mL
Code: 451W47IQ8X
Classification: IACT
Sodium bicarbonateInactive
Quantity: 0.125 g in 100 mL
Code: 8MDF5V39QO
Classification: IACT
GlycerinInactive
Quantity: 53 mL in 100 mL
Code: PDC6A3C0OX
Classification: IACT
PhenolInactive
Quantity: 0.4 g in 100 mL
Code: 339NCG44TV
Classification: IACT
WaterInactive
Code: 059QF0KO0R
Classification: IACT