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"58657-713-30" National Drug Code (NDC)

Bupropion Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (58657-713-30)
(Method Pharmaceuticals, LLC)

NDC Code58657-713-30
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (58657-713-30)
Product NDC58657-713
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20190128
End Marketing Date20231231
Marketing Category NameANDA
Application NumberANDA211020
ManufacturerMethod Pharmaceuticals, LLC
Substance NameBUPROPION HYDROCHLORIDE
Strength300
Strength Unitmg/1
Pharmacy ClassesAminoketone [EPC], Dopamine Uptake Inhibitors [MoA], Increased Dopamine Activity [PE], Increased Norepinephrine Activity [PE], Norepinephrine Uptake Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/58657-713-30





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