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"71335-0949-7" National Drug Code (NDC)

Baclofen 56 TABLET in 1 BOTTLE (71335-0949-7)
(Bryant Ranch Prepack)

NDC Code71335-0949-7
Package Description56 TABLET in 1 BOTTLE (71335-0949-7)
Product NDC71335-0949
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBaclofen
Non-Proprietary NameBaclofen
Dosage FormTABLET
UsageORAL
Start Marketing Date20180401
Marketing Category NameANDA
Application NumberANDA209102
ManufacturerBryant Ranch Prepack
Substance NameBACLOFEN
Strength20
Strength Unitmg/1
Pharmacy ClassesGABA A Agonists [MoA], GABA B Agonists [MoA], gamma-Aminobutyric Acid-ergic Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-0949-7





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