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Standardized Kentucky (June) Bluegrass
Standardized Kentucky (June) Bluegrass - 49288-0277-3 - (Standardized Kentucky (June) Bluegrass)
Drug Information of Standardized Kentucky (June) Bluegrass
| Product NDC: | 49288-0277 |
| Proprietary Name: | Standardized Kentucky (June) Bluegrass |
| Non Proprietary Name: | Standardized Kentucky (June) Bluegrass |
| Active Ingredient(s): | 100000 [BAU]/mL & nbsp; Standardized Kentucky (June) Bluegrass |
| Administration Route(s): | INTRADERMAL; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Standardized Kentucky (June) Bluegrass
| Product NDC: | 49288-0277 |
| Labeler Name: | Antigen Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA103421 |
| Marketing Category: | BLA |
| Start Marketing Date: | 19970613 |
Package Information of Standardized Kentucky (June) Bluegrass
| Package NDC: | 49288-0277-3 |
| Package Description: | 10 mL in 1 VIAL, MULTI-DOSE (49288-0277-3) |
NDC Information of Standardized Kentucky (June) Bluegrass
| NDC Code | 49288-0277-3 |
| Proprietary Name | Standardized Kentucky (June) Bluegrass |
| Package Description | 10 mL in 1 VIAL, MULTI-DOSE (49288-0277-3) |
| Product NDC | 49288-0277 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Standardized Kentucky (June) Bluegrass |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRADERMAL; SUBCUTANEOUS |
| Start Marketing Date | 19970613 |
| Marketing Category Name | BLA |
| Labeler Name | Antigen Laboratories, 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] |
