www.ndcvalidator.com
National Drug Code Lookup | NDC Directory | About | Feedback

"70518-2637-1" National Drug Code (NDC)

Bupropion Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-2637-1)
(REMEDYREPACK INC.)

NDC Code70518-2637-1
Package Description30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-2637-1)
Product NDC70518-2637
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Proprietary Name SuffixXl
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20200318
Marketing Category NameANDA
Application NumberANDA210015
ManufacturerREMEDYREPACK INC.
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-2637-1





Copyright © 2007-2024 www.ndcvalidator.com