Cumin - 49288-0155-1 - (Cumin)

Alphabetical Index


Drug Information of Cumin

Product NDC: 49288-0155
Proprietary Name: Cumin
Non Proprietary Name: Cumin
Active Ingredient(s): .05    g/mL & nbsp;   Cumin
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cumin

Product NDC: 49288-0155
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Cumin

Package NDC: 49288-0155-1
Package Description: 2 mL in 1 VIAL, MULTI-DOSE (49288-0155-1)

NDC Information of Cumin

NDC Code 49288-0155-1
Proprietary Name Cumin
Package Description 2 mL in 1 VIAL, MULTI-DOSE (49288-0155-1)
Product NDC 49288-0155
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cumin
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name CUMIN
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Plant Allergenic Extract [EPC],Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient],Plant Proteins [Chemical/Ingredient],Food Additives [Chemical/Ingredient]

Complete Information of Cumin


General Information