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"70518-2022-0" National Drug Code (NDC)
Bupropion Hydrochloride 30 POUCH in 1 BOX (70518-2022-0) > 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-2022-1)
(REMEDYREPACK INC.)
NDC Code
70518-2022-0
Package Description
30 POUCH in 1 BOX (70518-2022-0) > 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-2022-1)
Product NDC
70518-2022
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Bupropion Hydrochloride
Non-Proprietary Name
Bupropion Hydrochloride
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20190415
Marketing Category Name
ANDA
Application Number
ANDA090693
Manufacturer
REMEDYREPACK INC.
Substance Name
BUPROPION HYDROCHLORIDE
Strength
150
Strength Unit
mg/1
Pharmacy Classes
Aminoketone [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/70518-2022-0