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"49288-0071-1" National Drug Code (NDC)

Bay Leaf 2 mL in 1 VIAL, MULTI-DOSE (49288-0071-1)
(Antigen Laboratories, Inc.)

NDC Code49288-0071-1
Package Description2 mL in 1 VIAL, MULTI-DOSE (49288-0071-1)
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

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/49288-0071-1





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