71335-0877 NDC - BUPROPION HYDROCHLORIDE ()

Drug Information

Product NDC: 71335-0877

Proprietary Name: bupropion Hydrochloride

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

No.	Package Code	Package Description
1	71335-0877-1	60 TABLET in 1 BOTTLE (71335-0877-1)
2	71335-0877-2	30 TABLET in 1 BOTTLE (71335-0877-2)
3	71335-0877-3	100 TABLET in 1 BOTTLE (71335-0877-3)
4	71335-0877-4	90 TABLET in 1 BOTTLE (71335-0877-4)
5	71335-0877-5	120 TABLET in 1 BOTTLE (71335-0877-5)
6	71335-0877-6	15 TABLET in 1 BOTTLE (71335-0877-6)
7	71335-0877-7	21 TABLET in 1 BOTTLE (71335-0877-7)

Field Name	Field Value	Definition
PRODUCT NDC	71335-0877	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAME	bupropion Hydrochloride	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	5/26/2018	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Bryant Ranch Prepack	Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 4/12/2024