NDC 36987-1910 Botrytis Cinerea
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 36987 - Nelco Laboratories, Inc.
- 36987-1910 - Botrytis Cinerea
Product Packages
NDC Code 36987-1910-1
Package Description: 5 mL in 1 VIAL, MULTI-DOSE
NDC Code 36987-1910-2
Package Description: 10 mL in 1 VIAL, MULTI-DOSE
NDC Code 36987-1910-3
Package Description: 30 mL in 1 VIAL, MULTI-DOSE
NDC Code 36987-1910-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE
Product Details
What is NDC 36987-1910?
What are the uses for Botrytis Cinerea?
Which are Botrytis Cinerea UNII Codes?
The UNII codes for the active ingredients in this product are:
- ASPERGILLUS FUMIGATUS (UNII: X88DF51T48)
- ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (Active Moiety)
- ALTERNARIA ALTERNATA (UNII: 52B29REC7H)
- ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (Active Moiety)
- ASPERGILLUS FLAVUS (UNII: 3J888Y9L13)
- ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (Active Moiety)
- EUROTIUM HERBARIORUM (UNII: 49W168AES4)
- EUROTIUM HERBARIORUM (UNII: 49W168AES4) (Active Moiety)
- ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6)
- ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (Active Moiety)
- ASPERGILLUS TERREUS (UNII: QBN8K7055X)
- ASPERGILLUS TERREUS (UNII: QBN8K7055X) (Active Moiety)
- BOTRYTIS CINEREA (UNII: TBW53313S7)
- BOTRYTIS CINEREA (UNII: TBW53313S7) (Active Moiety)
Which are Botrytis Cinerea Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- PHENOL (UNII: 339NCG44TV)
What is the NDC to RxNorm Crosswalk for Botrytis Cinerea?
- RxCUI: 1006290 - Aspergillus flavus allergenic extract 100 MG/ML Injectable Solution
- RxCUI: 1006290 - Aspergillus flavus allergenic extract 0.1 GM/ML Injectable Solution
- RxCUI: 1006326 - Aspergillus terreus allergenic extract 100 MG/ML Injectable Solution
- RxCUI: 1006326 - Aspergillus terreus allergenic extract 0.1 GM/ML Injectable Solution
- RxCUI: 1010906 - Geotrichum candidum allergenic extract 100 MG/ML Injectable Solution
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".