NDC 22840-1678

Fusarium solani

Fusarium Solani

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 ID22840-1678_77436178-2957-6a77-e053-2a91aa0a873e
NDC22840-1678
Product TypeNon-standardized Allergenic
Proprietary NameFusarium solani
Generic NameFusarium Solani
Dosage FormSolution
Route of AdministrationINTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS
Marketing Start Date1981-09-15
Marketing CategoryBLA / BLA
Application NumberBLA101833
Labeler NameGreer Laboratories, Inc.
Substance NameHAEMATONECTRIA HAEMATOCOCCA
Active Ingredient Strength0 g/mL
Pharm ClassesNon-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [CS],Allergens [CS]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 22840-1678-1

5 mL in 1 VIAL, MULTI-DOSE (22840-1678-1)
Marketing Start Date1981-09-15
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 22840-1678-1 [22840167801]

Fusarium solani SOLUTION
Marketing CategoryBLA
Application NumberBLA101833
Product TypeNON-STANDARDIZED ALLERGENIC
Marketing Start Date1981-09-15

Drug Details

Active Ingredients

IngredientStrength
HAEMATONECTRIA HAEMATOCOCCA.001 g/mL

Pharmacological Class

  • Non-Standardized Fungal Allergenic Extract [EPC]
  • Increased Histamine Release [PE]
  • Cell-mediated Immunity [PE]
  • Increased IgG Production [PE]
  • Fungal Proteins [CS]
  • Allergens [CS]

NDC Crossover Matching brand name "Fusarium solani" or generic name "Fusarium Solani"

NDCBrand NameGeneric Name
22840-1676Fusarium solaniFusarium solani
22840-1677Fusarium solaniFusarium solani
22840-1678Fusarium solaniFusarium solani
22840-5619Fusarium solaniFusarium solani
54575-197FUSARIUM SOLANIhaematonectria haematococca
49643-111FusariumFusarium solani

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