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"70518-2648-0" National Drug Code (NDC)
Bupropion Hydrochloride (sr) 30 POUCH in 1 BOX (70518-2648-0) > 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-2648-1)
(REMEDYREPACK INC.)
NDC Code
70518-2648-0
Package Description
30 POUCH in 1 BOX (70518-2648-0) > 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-2648-1)
Product NDC
70518-2648
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Bupropion Hydrochloride (sr)
Non-Proprietary Name
Bupropion Hydrochloride
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20200324
Marketing Category Name
ANDA
Application Number
ANDA206122
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/70518-2648-0