"36987-1669-3" National Drug Code (NDC)

Bay Leaf 30 mL in 1 VIAL, MULTI-DOSE (36987-1669-3)
(Nelco Laboratories, Inc.)

NDC Code36987-1669-3
Package Description30 mL in 1 VIAL, MULTI-DOSE (36987-1669-3)
Product NDC36987-1669
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBay Leaf
Non-Proprietary NameBay Leaf
Dosage FormINJECTION, SOLUTION
UsageINTRADERMAL; SUBCUTANEOUS
Start Marketing Date19720829
Marketing Category NameBLA
Application NumberBLA102192
ManufacturerNelco Laboratories, Inc.
Substance NameLAURUS NOBILIS
Strength.1
Strength Unitg/mL

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