Crab - 49288-0119-5 - (Crab)

Alphabetical Index


Drug Information of Crab

Product NDC: 49288-0119
Proprietary Name: Crab
Non Proprietary Name: Crab
Active Ingredient(s): .05    g/mL & nbsp;   Crab
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Crab

Product NDC: 49288-0119
Labeler Name: Antigen Laboratories, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 20110722

Package Information of Crab

Package NDC: 49288-0119-5
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (49288-0119-5)

NDC Information of Crab

NDC Code 49288-0119-5
Proprietary Name Crab
Package Description 50 mL in 1 VIAL, MULTI-DOSE (49288-0119-5)
Product NDC 49288-0119
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Crab
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 20110722
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name OPILIO CRAB
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes

Complete Information of Crab


General Information