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STANDARDIZED PERENNIAL RYEGRASS GRASS POLLEN
STANDARDIZED PERENNIAL RYEGRASS GRASS POLLEN - 54575-102-50 - (Lolium perenne pollen)
Drug Information of STANDARDIZED PERENNIAL RYEGRASS GRASS POLLEN
| Product NDC: | 54575-102 |
| Proprietary Name: | STANDARDIZED PERENNIAL RYEGRASS GRASS POLLEN |
| Non Proprietary Name: | Lolium perenne pollen |
| Active Ingredient(s): | 100000 [BAU]/mL & nbsp; Lolium perenne pollen |
| Administration Route(s): | PERCUTANEOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of STANDARDIZED PERENNIAL RYEGRASS GRASS POLLEN
| Product NDC: | 54575-102 |
| Labeler Name: | Allergy Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA101384 |
| Marketing Category: | BLA |
| Start Marketing Date: | 19970625 |
Package Information of STANDARDIZED PERENNIAL RYEGRASS GRASS POLLEN
| Package NDC: | 54575-102-50 |
| Package Description: | 50 mL in 1 VIAL, MULTI-DOSE (54575-102-50) |
NDC Information of STANDARDIZED PERENNIAL RYEGRASS GRASS POLLEN
| NDC Code | 54575-102-50 |
| Proprietary Name | STANDARDIZED PERENNIAL RYEGRASS GRASS POLLEN |
| Package Description | 50 mL in 1 VIAL, MULTI-DOSE (54575-102-50) |
| Product NDC | 54575-102 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Lolium perenne pollen |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | PERCUTANEOUS; SUBCUTANEOUS |
| Start Marketing Date | 19970625 |
| Marketing Category Name | BLA |
| Labeler Name | Allergy Laboratories, Inc. |
| Substance Name | LOLIUM PERENNE POLLEN |
| Strength Number | 100000 |
| Strength Unit | [BAU]/mL |
| Pharmaceutical Classes | Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient] |
