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Timothy, Standardized
Timothy, Standardized - 0268-0279-50 - (Timothy, Standardized)
Drug Information of Timothy, Standardized
| Product NDC: | 0268-0279 |
| Proprietary Name: | Timothy, Standardized |
| Non Proprietary Name: | Timothy, Standardized |
| Active Ingredient(s): | 100000 [BAU]/mL & nbsp; Timothy, Standardized |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Timothy, Standardized
| Product NDC: | 0268-0279 |
| Labeler Name: | ALK-Abello, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA103058 |
| Marketing Category: | BLA |
| Start Marketing Date: | 19971218 |
Package Information of Timothy, Standardized
| Package NDC: | 0268-0279-50 |
| Package Description: | 50 mL in 1 VIAL, MULTI-DOSE (0268-0279-50) |
NDC Information of Timothy, Standardized
| NDC Code | 0268-0279-50 |
| Proprietary Name | Timothy, Standardized |
| Package Description | 50 mL in 1 VIAL, MULTI-DOSE (0268-0279-50) |
| Product NDC | 0268-0279 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Timothy, Standardized |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 19971218 |
| Marketing Category Name | BLA |
| Labeler Name | ALK-Abello, Inc. |
| Substance Name | PHLEUM PRATENSE 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] |
