Arabic Gum - 36987-1640-3 - (Arabic Gum)

Alphabetical Index


Drug Information of Arabic Gum

Product NDC: 36987-1640
Proprietary Name: Arabic Gum
Non Proprietary Name: Arabic Gum
Active Ingredient(s): .01    g/mL & nbsp;   Arabic Gum
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Arabic Gum

Product NDC: 36987-1640
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Arabic Gum

Package NDC: 36987-1640-3
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (36987-1640-3)

NDC Information of Arabic Gum

NDC Code 36987-1640-3
Proprietary Name Arabic Gum
Package Description 30 mL in 1 VIAL, MULTI-DOSE (36987-1640-3)
Product NDC 36987-1640
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Arabic Gum
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name ACACIA
Strength Number .01
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Plant Proteins [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of Arabic Gum


General Information