Nigrospora sphaerica
Allergenic Extract
Approved
Approval ID
cf7177af-9b37-4aba-af3d-f5f4a95bf117
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 14, 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.
Nigrospora sphaerica
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-2025
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Nigrospora sphaerica
Product Specifications
Route of AdministrationSUBCUTANEOUS, INTRADERMAL
Effective DateDecember 14, 2009
FDA Product Classification
INGREDIENTS (6)
KHUSKIA ORYZAEActive
Quantity: 0.05 g in 1 mL
Code: VK8C112WTS
Classification: ACTIB
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
GLYCERINInactive
Code: PDC6A3C0OX
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT