Botrytis cinerea is a Intradermal; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Nelco Laboratories, Inc.. The primary component is Botrytis Cinerea.
| Product ID | 36987-1903_a9a7717a-fa1d-462b-b0eb-5f1993dba6a3 | 
| NDC | 36987-1903 | 
| Product Type | Human Prescription Drug | 
| Proprietary Name | Botrytis cinerea | 
| Generic Name | Botrytis Cinerea | 
| Dosage Form | Injection, Solution | 
| Route of Administration | INTRADERMAL; SUBCUTANEOUS | 
| Marketing Start Date | 1972-08-29 | 
| Marketing Category | BLA / BLA | 
| Application Number | BLA102192 | 
| Labeler Name | Nelco Laboratories, Inc. | 
| Substance Name | BOTRYTIS CINEREA | 
| Active Ingredient Strength | 10000 [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 | E | 
| Listing Certified Through | 2017-12-31 | 
| Marketing Start Date | 1972-08-29 | 
| NDC Exclude Flag | N | 
| Sample Package? | N | 
| Marketing Category | BLA | 
| Application Number | BLA102192 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 1972-08-29 | 
| Inactivation Date | 2019-10-21 | 
| Marketing Category | BLA | 
| Application Number | BLA102192 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 1972-08-29 | 
| Inactivation Date | 2019-10-21 | 
| Marketing Category | BLA | 
| Application Number | BLA102192 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 1972-08-29 | 
| Inactivation Date | 2019-10-21 | 
| Marketing Category | BLA | 
| Application Number | BLA102192 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 1972-08-29 | 
| Inactivation Date | 2019-10-21 | 
| Ingredient | Strength | 
|---|---|
| BOTRYTIS CINEREA | 10000 [PNU]/mL | 
| SPL SET ID: | e464ea5b-a803-4c5a-93d2-cc3fbca8d3a8 | 
| Manufacturer | |
| UNII | 
 | 
| RxNorm Concept Unique ID - RxCUI | |
| Pharm Class PE | |
| PHarm Class EPC | |
| NUI Code | 
| NDC | Brand Name | Generic Name | 
|---|---|---|
| 0268-0837 | BOTRYTIS CINEREA | BOTRYTIS CINEREA | 
| 0268-0838 | BOTRYTIS CINEREA | BOTRYTIS CINEREA | 
| 0268-0839 | BOTRYTIS CINEREA | BOTRYTIS CINEREA | 
| 0268-0840 | BOTRYTIS CINEREA | BOTRYTIS CINEREA | 
| 0268-0841 | BOTRYTIS CINEREA | BOTRYTIS CINEREA | 
| 0268-6512 | BOTRYTIS CINEREA | Botrytis cinerea | 
| 0268-6513 | BOTRYTIS CINEREA | Botrytis cinerea | 
| 0268-8090 | BOTRYTIS CINEREA | BOTRYTIS CINEREA | 
| 0268-8091 | BOTRYTIS CINEREA | BOTRYTIS CINEREA | 
| 22840-1639 | Botrytis cinerea | Botrytis cinerea | 
| 22840-2662 | Botrytis cinerea | Botrytis cinerea | 
| 22840-5609 | Botrytis cinerea | Botrytis cinerea | 
| 36987-1902 | Botrytis cinerea | Botrytis cinerea | 
| 36987-1903 | Botrytis cinerea | Botrytis cinerea | 
| 36987-1904 | Botrytis cinerea | Botrytis cinerea | 
| 36987-1907 | Botrytis cinerea | Botrytis cinerea | 
| 36987-1909 | Botrytis cinerea | Botrytis cinerea | 
| 36987-1905 | Botrytis cinerea | Botrytis cinerea | 
| 36987-1908 | Botrytis cinerea | Botrytis cinerea | 
| 36987-1906 | Botrytis cinerea | Botrytis cinerea | 
| 36987-1910 | Botrytis cinerea | Botrytis cinerea | 
| 54575-187 | BOTRYTIS CINEREA | BOTRYTIS CINEREA |