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"31722-068-05" National Drug Code (NDC)

Bupropion Hydrochloride 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-068-05)
(Camber Pharmaceuticals, Inc.)

NDC Code31722-068-05
Package Description500 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-068-05)
Product NDC31722-068
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20230531
Marketing Category NameANDA
Application NumberANDA216800
ManufacturerCamber Pharmaceuticals, Inc.
Substance NameBUPROPION HYDROCHLORIDE
Strength200
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/31722-068-05





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