Millet - 49288-0303-5 - (Millet)

Alphabetical Index


Drug Information of Millet

Product NDC: 49288-0303
Proprietary Name: Millet
Non Proprietary Name: Millet
Active Ingredient(s): .05    g/mL & nbsp;   Millet
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Millet

Product NDC: 49288-0303
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Millet

Package NDC: 49288-0303-5
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (49288-0303-5)

NDC Information of Millet

NDC Code 49288-0303-5
Proprietary Name Millet
Package Description 50 mL in 1 VIAL, MULTI-DOSE (49288-0303-5)
Product NDC 49288-0303
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Millet
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name MILLET SEED
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes

Complete Information of Millet


General Information