"69844-011-02" National Drug Code (NDC)

Bupropion Hydrochloride 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (69844-011-02)
(Graviti Pharmaceuticals Private Limited)

NDC Code69844-011-02
Package Description90 TABLET, EXTENDED RELEASE in 1 BOTTLE (69844-011-02)
Product NDC69844-011
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
Strength150
Strength Unitmg/1
Pharmacy ClassesAminoketone [EPC], Dopamine Uptake Inhibitors [MoA], Increased Dopamine Activity [PE], Increased Norepinephrine Activity [PE], Norepinephrine Uptake Inhibitors [MoA]

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