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"69844-064-01" National Drug Code (NDC)
Bupropion Hydrochloride 30 TABLET in 1 BOTTLE (69844-064-01)
(Graviti Pharmaceuticals Private Limited)
NDC Code
69844-064-01
Package Description
30 TABLET in 1 BOTTLE (69844-064-01)
Product NDC
69844-064
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Bupropion Hydrochloride
Non-Proprietary Name
Extended-release
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20190128
Marketing Category Name
ANDA
Application Number
ANDA211020
Manufacturer
Graviti Pharmaceuticals Private Limited
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/69844-064-01