Bluefish
Allergenic Extract
Approved
Approval ID
501aa718-e787-44a0-aa7f-dddf7446ac6e
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 10, 2009
Manufacturers
FDA
Nelco Laboratories, Inc.
DUNS: 054980867
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Bluefish
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-1190
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Bluefish
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 10, 2009
FDA Product Classification
INGREDIENTS (5)
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
BLUEFISHActive
Quantity: 0.05 g in 1 mL
Code: 79U8P8X3Q5
Classification: ACTIB
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT