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Candin
Candin - 49643-138-01 - (Candida albicans Skin Test Antigen)
Drug Information of Candin
| Product NDC: | 49643-138 |
| Proprietary Name: | Candin |
| Non Proprietary Name: | Candida albicans Skin Test Antigen |
| Active Ingredient(s): | 1 U/.1mL & nbsp; Candida albicans Skin Test Antigen |
| Administration Route(s): | INTRADERMAL |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Candin
| Product NDC: | 49643-138 |
| Labeler Name: | Allermed Laboratories, Inc. |
| Product Type: | STANDARDIZED ALLERGENIC |
| FDA Application Number: | BLA103257 |
| Marketing Category: | BLA |
| Start Marketing Date: | 19951201 |
Package Information of Candin
| Package NDC: | 49643-138-01 |
| Package Description: | 1 mL in 1 VIAL, MULTI-DOSE (49643-138-01) |
NDC Information of Candin
| NDC Code | 49643-138-01 |
| Proprietary Name | Candin |
| Package Description | 1 mL in 1 VIAL, MULTI-DOSE (49643-138-01) |
| Product NDC | 49643-138 |
| Product Type Name | STANDARDIZED ALLERGENIC |
| Non Proprietary Name | Candida albicans Skin Test Antigen |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRADERMAL |
| Start Marketing Date | 19951201 |
| Marketing Category Name | BLA |
| Labeler Name | Allermed Laboratories, Inc. |
| Substance Name | CANDIDA ALBICANS |
| Strength Number | 1 |
| Strength Unit | U/.1mL |
| Pharmaceutical Classes | Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [Chemical/Ingredient],Allergens [Chemical/Ingredient],Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE] |
