Parakeet Feather
Allergenic Extract
Approved
Approval ID
eb2f0512-0060-4508-a4ea-2ddd73396cdd
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 20, 2009
Manufacturers
FDA
Antigen Laboratories, Inc.
DUNS: 030705628
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Parakeet Feather
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code49288-0390
Application NumberBLA102223
Product Classification
M
Marketing Category
C73585
G
Generic Name
Parakeet Feather
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateNovember 20, 2009
FDA Product Classification
INGREDIENTS (5)
MELOPSITTACUS UNDULATUS FEATHERActive
Quantity: 0.02 g in 1 mL
Code: 1XY644QKWG
Classification: ACTIB
GLYCERINInactive
Quantity: 0.525 mL in 1 mL
Code: PDC6A3C0OX
Classification: IACT
SODIUM CHLORIDEInactive
Quantity: 0.0095 g in 1 mL
Code: 451W47IQ8X
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM BICARBONATEInactive
Quantity: 0.0024 g in 1 mL
Code: 8MDF5V39QO
Classification: IACT
Drug Labeling Information
BOXED WARNING SECTION
LOINC: 34066-1Updated: 11/20/2009