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Phoma glomerata - 36987-2059-1 - (Phoma glomerata)

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Drug Information of Phoma glomerata

Product NDC: 36987-2059
Proprietary Name: Phoma glomerata
Non Proprietary Name: Phoma glomerata
Active Ingredient(s): 40000    [PNU]/mL & nbsp;   Phoma glomerata
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Phoma glomerata

Product NDC: 36987-2059
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Phoma glomerata

Package NDC: 36987-2059-1
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (36987-2059-1)

NDC Information of Phoma glomerata

NDC Code 36987-2059-1
Proprietary Name Phoma glomerata
Package Description 5 mL in 1 VIAL, MULTI-DOSE (36987-2059-1)
Product NDC 36987-2059
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Phoma glomerata
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name PHOMA GLOMERATA
Strength Number 40000
Strength Unit [PNU]/mL
Pharmaceutical Classes

Complete Information of Phoma glomerata


General Information