NDC 22840-5632
Phoma betae
Phoma Betae
Phoma betae 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 Pleospora Betae.
| Product ID | 22840-5632_77436178-2957-6a77-e053-2a91aa0a873e |
| NDC | 22840-5632 |
| Product Type | Non-standardized Allergenic |
| Proprietary Name | Phoma betae |
| Generic Name | Phoma Betae |
| 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 | PLEOSPORA BETAE |
| Active Ingredient Strength | 0 g/mL |
| Pharm Classes | Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [CS],Allergens [CS],Non-Standardized Fungal Allergenic Extract [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |