Bay Leaf - 36987-1666-3 - (Bay Leaf)

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Drug Information of Bay Leaf

Product NDC: 36987-1666
Proprietary Name: Bay Leaf
Non Proprietary Name: Bay Leaf
Active Ingredient(s): .05    g/mL & nbsp;   Bay Leaf
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Bay Leaf

Product NDC: 36987-1666
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Bay Leaf

Package NDC: 36987-1666-3
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (36987-1666-3)

NDC Information of Bay Leaf

NDC Code 36987-1666-3
Proprietary Name Bay Leaf
Package Description 30 mL in 1 VIAL, MULTI-DOSE (36987-1666-3)
Product NDC 36987-1666
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bay Leaf
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name LAURUS NOBILIS
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes

Complete Information of Bay Leaf


General Information