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Kentucky Bluegrass (June), Standardized
Kentucky Bluegrass (June), Standardized - 0268-3051-06 - (Kentucky Bluegrass (June), Standardized)
Drug Information of Kentucky Bluegrass (June), Standardized
| Product NDC: | 0268-3051 |
| Proprietary Name: | Kentucky Bluegrass (June), Standardized |
| Non Proprietary Name: | Kentucky Bluegrass (June), Standardized |
| Active Ingredient(s): | 100000 [BAU]/mL & nbsp; Kentucky Bluegrass (June), Standardized |
| Administration Route(s): | PERCUTANEOUS |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Kentucky Bluegrass (June), Standardized
| Product NDC: | 0268-3051 |
| Labeler Name: | ALK-Abello, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA103052 |
| Marketing Category: | BLA |
| Start Marketing Date: | 19971218 |
Package Information of Kentucky Bluegrass (June), Standardized
| Package NDC: | 0268-3051-06 |
| Package Description: | 5 mL in 1 VIAL, MULTI-DOSE (0268-3051-06) |
NDC Information of Kentucky Bluegrass (June), Standardized
| NDC Code | 0268-3051-06 |
| Proprietary Name | Kentucky Bluegrass (June), Standardized |
| Package Description | 5 mL in 1 VIAL, MULTI-DOSE (0268-3051-06) |
| Product NDC | 0268-3051 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Kentucky Bluegrass (June), Standardized |
| Dosage Form Name | SOLUTION |
| Route Name | PERCUTANEOUS |
| Start Marketing Date | 19971218 |
| Marketing Category Name | BLA |
| Labeler Name | ALK-Abello, Inc. |
| Substance Name | POA PRATENSIS 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] |
