"49288-0071-5" National Drug Code (NDC)

Bay Leaf 50 mL in 1 VIAL, MULTI-DOSE (49288-0071-5)
(Antigen Laboratories, Inc.)

NDC Code49288-0071-5
Package Description50 mL in 1 VIAL, MULTI-DOSE (49288-0071-5)
Product NDC49288-0071
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBay Leaf
Non-Proprietary NameBay Leaf
Dosage FormINJECTION, SOLUTION
UsageINTRADERMAL; SUBCUTANEOUS
Start Marketing Date19740323
Marketing Category NameBLA
Application NumberBLA102223
ManufacturerAntigen Laboratories, Inc.
Substance NameLAURUS NOBILIS
Strength.05
Strength Unitg/mL

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