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Standardized Redtop Grass
Standardized Redtop Grass - 49643-309-30 - (Agrostis alba)
Drug Information of Standardized Redtop Grass
| Product NDC: | 49643-309 |
| Proprietary Name: | Standardized Redtop Grass |
| Non Proprietary Name: | Agrostis alba |
| Active Ingredient(s): | 100000 [BAU]/mL & nbsp; Agrostis alba |
| Administration Route(s): | CUTANEOUS; INTRADERMAL; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Standardized Redtop Grass
| Product NDC: | 49643-309 |
| Labeler Name: | Allermed Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA102218 |
| Marketing Category: | BLA |
| Start Marketing Date: | 19961202 |
Package Information of Standardized Redtop Grass
| Package NDC: | 49643-309-30 |
| Package Description: | 30 mL in 1 VIAL, MULTI-DOSE (49643-309-30) |
NDC Information of Standardized Redtop Grass
| NDC Code | 49643-309-30 |
| Proprietary Name | Standardized Redtop Grass |
| Package Description | 30 mL in 1 VIAL, MULTI-DOSE (49643-309-30) |
| Product NDC | 49643-309 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Agrostis alba |
| Dosage Form Name | INJECTION |
| Route Name | CUTANEOUS; INTRADERMAL; SUBCUTANEOUS |
| Start Marketing Date | 19961202 |
| Marketing Category Name | BLA |
| Labeler Name | Allermed Laboratories, Inc. |
| Substance Name | AGROSTIS GIGANTEA POLLEN |
| Strength Number | 100000 |
| Strength Unit | [BAU]/mL |
| Pharmaceutical Classes | Standardized Pollen Allergenic Extract [EPC],Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient] |
