Nigrospora sphaerica
Allergenic Extract
Approved
Approval ID
39df21dd-b3f0-4f12-94c5-222e41c5ebba
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
NDC Product Code36987-2024
Application NumberBLA102192
Marketing CategoryC73585
Route of AdministrationSUBCUTANEOUS, INTRADERMAL
Effective DateDecember 14, 2009
Generic NameNigrospora sphaerica
INGREDIENTS (5)
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
KHUSKIA ORYZAEActive
Quantity: 0.05 g in 1 mL
Code: VK8C112WTS
Classification: ACTIB
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT