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"68071-1311-3" National Drug Code (NDC)
Bupropion Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-1311-3)
(NuCare Pharmaceuticals,Inc.)
NDC Code
68071-1311-3
Package Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-1311-3)
Product NDC
68071-1311
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
20190325
Marketing Category Name
ANDA
Application Number
ANDA210497
Manufacturer
NuCare Pharmaceuticals,Inc.
Substance Name
BUPROPION HYDROCHLORIDE
Strength
300
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/68071-1311-3