Thompson Seedless Grape
Allergenic Extract
Approved
Approval ID
4820970d-3c16-43b9-b919-83e47a2dd246
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 9, 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.
Thompson Seedless Grape
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-1327
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Thompson Seedless Grape
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 9, 2009
FDA Product Classification
INGREDIENTS (6)
WINE GRAPEActive
Quantity: 0.05 g in 1 mL
Code: 3GOV20705G
Classification: ACTIB
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
GLYCERINInactive
Code: PDC6A3C0OX
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT