Fusarium solani is a Intradermal; Percutaneous; Subcutaneous Solution in the Non-standardized Allergenic category. It is labeled and distributed by Greer Laboratories, Inc.. The primary component is Haematonectria Haematococca.
| Product ID | 22840-1677_77436178-2957-6a77-e053-2a91aa0a873e |
| NDC | 22840-1677 |
| Product Type | Non-standardized Allergenic |
| Proprietary Name | Fusarium solani |
| Generic Name | Fusarium Solani |
| Dosage Form | Solution |
| Route of Administration | INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS |
| Marketing Start Date | 1981-09-15 |
| Marketing Category | BLA / BLA |
| Application Number | BLA101833 |
| Labeler Name | Greer Laboratories, Inc. |
| Substance Name | HAEMATONECTRIA HAEMATOCOCCA |
| Active Ingredient Strength | 20000 [PNU]/mL |
| Pharm Classes | Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [CS],Allergens [CS] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 1981-09-15 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | BLA |
| Application Number | BLA101833 |
| Product Type | NON-STANDARDIZED ALLERGENIC |
| Marketing Start Date | 1981-09-15 |
| Ingredient | Strength |
|---|---|
| HAEMATONECTRIA HAEMATOCOCCA | 20000 [PNU]/mL |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 22840-1676 | Fusarium solani | Fusarium solani |
| 22840-1677 | Fusarium solani | Fusarium solani |
| 22840-1678 | Fusarium solani | Fusarium solani |
| 22840-5619 | Fusarium solani | Fusarium solani |
| 54575-197 | FUSARIUM SOLANI | haematonectria haematococca |
| 49643-111 | Fusarium | Fusarium solani |