Salt Grass - 36987-2398-3 - (Salt Grass)

Alphabetical Index


Drug Information of Salt Grass

Product NDC: 36987-2398
Proprietary Name: Salt Grass
Non Proprietary Name: Salt Grass
Active Ingredient(s): .1    g/mL & nbsp;   Salt Grass
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Salt Grass

Product NDC: 36987-2398
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Salt Grass

Package NDC: 36987-2398-3
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (36987-2398-3)

NDC Information of Salt Grass

NDC Code 36987-2398-3
Proprietary Name Salt Grass
Package Description 30 mL in 1 VIAL, MULTI-DOSE (36987-2398-3)
Product NDC 36987-2398
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Salt Grass
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name DISTICHLIS SPICATA POLLEN
Strength Number .1
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 Salt Grass


General Information