Nectarine - 36987-1591-3 - (Nectarine)

Alphabetical Index


Drug Information of Nectarine

Product NDC: 36987-1591
Proprietary Name: Nectarine
Non Proprietary Name: Nectarine
Active Ingredient(s): .05    g/mL & nbsp;   Nectarine
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Nectarine

Product NDC: 36987-1591
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Nectarine

Package NDC: 36987-1591-3
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (36987-1591-3)

NDC Information of Nectarine

NDC Code 36987-1591-3
Proprietary Name Nectarine
Package Description 30 mL in 1 VIAL, MULTI-DOSE (36987-1591-3)
Product NDC 36987-1591
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nectarine
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name NECTARINE
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes

Complete Information of Nectarine


General Information