Saltgrass - 49288-0494-5 - (Saltgrass)

Alphabetical Index


Drug Information of Saltgrass

Product NDC: 49288-0494
Proprietary Name: Saltgrass
Non Proprietary Name: Saltgrass
Active Ingredient(s): .05    g/mL & nbsp;   Saltgrass
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Saltgrass

Product NDC: 49288-0494
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Saltgrass

Package NDC: 49288-0494-5
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (49288-0494-5)

NDC Information of Saltgrass

NDC Code 49288-0494-5
Proprietary Name Saltgrass
Package Description 50 mL in 1 VIAL, MULTI-DOSE (49288-0494-5)
Product NDC 49288-0494
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Saltgrass
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name DISTICHLIS SPICATA POLLEN
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of Saltgrass


General Information