Blackberry - 36987-1300-4 - (Blackberry)

Alphabetical Index


Drug Information of Blackberry

Product NDC: 36987-1300
Proprietary Name: Blackberry
Non Proprietary Name: Blackberry
Active Ingredient(s): .1    g/mL & nbsp;   Blackberry
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Blackberry

Product NDC: 36987-1300
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Blackberry

Package NDC: 36987-1300-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (36987-1300-4)

NDC Information of Blackberry

NDC Code 36987-1300-4
Proprietary Name Blackberry
Package Description 50 mL in 1 VIAL, MULTI-DOSE (36987-1300-4)
Product NDC 36987-1300
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Blackberry
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name BLACKBERRY
Strength Number .1
Strength Unit g/mL
Pharmaceutical Classes

Complete Information of Blackberry


General Information