Radish - 49288-0438-3 - (Radish)

Alphabetical Index


Drug Information of Radish

Product NDC: 49288-0438
Proprietary Name: Radish
Non Proprietary Name: Radish
Active Ingredient(s): .05    g/mL & nbsp;   Radish
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Radish

Product NDC: 49288-0438
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Radish

Package NDC: 49288-0438-3
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (49288-0438-3)

NDC Information of Radish

NDC Code 49288-0438-3
Proprietary Name Radish
Package Description 10 mL in 1 VIAL, MULTI-DOSE (49288-0438-3)
Product NDC 49288-0438
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Radish
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name RAPHANUS SATIVUS
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes

Complete Information of Radish


General Information