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CENTER-AL - BETULA LENTA POLLEN
CENTER-AL - BETULA LENTA POLLEN - 0268-0041-30 - (Allergenic Extracts Alum Precipitated)
Drug Information of CENTER-AL - BETULA LENTA POLLEN
| Product NDC: | 0268-0041 |
| Proprietary Name: | CENTER-AL - BETULA LENTA POLLEN |
| Non Proprietary Name: | Allergenic Extracts Alum Precipitated |
| Active Ingredient(s): | 10000 [PNU]/mL & nbsp; Allergenic Extracts Alum Precipitated |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CENTER-AL - BETULA LENTA POLLEN
| Product NDC: | 0268-0041 |
| Labeler Name: | ALK-Abello, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA103753 |
| Marketing Category: | BLA |
| Start Marketing Date: | 19750115 |
Package Information of CENTER-AL - BETULA LENTA POLLEN
| Package NDC: | 0268-0041-30 |
| Package Description: | 30 mL in 1 VIAL, MULTI-DOSE (0268-0041-30) |
NDC Information of CENTER-AL - BETULA LENTA POLLEN
| NDC Code | 0268-0041-30 |
| Proprietary Name | CENTER-AL - BETULA LENTA POLLEN |
| Package Description | 30 mL in 1 VIAL, MULTI-DOSE (0268-0041-30) |
| Product NDC | 0268-0041 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Allergenic Extracts Alum Precipitated |
| Dosage Form Name | INJECTION, SUSPENSION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 19750115 |
| Marketing Category Name | BLA |
| Labeler Name | ALK-Abello, Inc. |
| Substance Name | BETULA LENTA POLLEN |
| Strength Number | 10000 |
| Strength Unit | [PNU]/mL |
| Pharmaceutical Classes | Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient] |
