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"69844-010-03" National Drug Code (NDC)

Bupropion Hydrochloride 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (69844-010-03)
(Graviti Pharmaceuticals Private Limited)

NDC Code69844-010-03
Package Description1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (69844-010-03)
Product NDC69844-010
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20190128
Marketing Category NameANDA
Application NumberANDA211020
ManufacturerGraviti Pharmaceuticals Private Limited
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/69844-010-03





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