Product NDC: | 36987-2235 |
Proprietary Name: | Orris Root |
Non Proprietary Name: | Orris Root |
Active Ingredient(s): | .05 g/mL & nbsp; Orris Root |
Administration Route(s): | INTRADERMAL; SUBCUTANEOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 36987-2235 |
Labeler Name: | Nelco Laboratories, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | BLA102192 |
Marketing Category: | BLA |
Start Marketing Date: | 19720829 |
Package NDC: | 36987-2235-3 |
Package Description: | 30 mL in 1 VIAL, MULTI-DOSE (36987-2235-3) |
NDC Code | 36987-2235-3 |
Proprietary Name | Orris Root |
Package Description | 30 mL in 1 VIAL, MULTI-DOSE (36987-2235-3) |
Product NDC | 36987-2235 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Orris Root |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRADERMAL; SUBCUTANEOUS |
Start Marketing Date | 19720829 |
Marketing Category Name | BLA |
Labeler Name | Nelco Laboratories, Inc. |
Substance Name | IRIS GERMANICA VAR. FLORENTINA ROOT |
Strength Number | .05 |
Strength Unit | g/mL |
Pharmaceutical Classes | Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [Chemical/Ingredient],Non-Standardized Plant Allergenic Extract [EPC],Plant Proteins [Chemical/Ingredient] |