Mackerel - 36987-1232-3 - (Mackerel)

Alphabetical Index


Drug Information of Mackerel

Product NDC: 36987-1232
Proprietary Name: Mackerel
Non Proprietary Name: Mackerel
Active Ingredient(s): .1    g/mL & nbsp;   Mackerel
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Mackerel

Product NDC: 36987-1232
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Mackerel

Package NDC: 36987-1232-3
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (36987-1232-3)

NDC Information of Mackerel

NDC Code 36987-1232-3
Proprietary Name Mackerel
Package Description 30 mL in 1 VIAL, MULTI-DOSE (36987-1232-3)
Product NDC 36987-1232
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mackerel
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name MACKEREL
Strength Number .1
Strength Unit g/mL
Pharmaceutical Classes

Complete Information of Mackerel


General Information