55648-105 NDC - BUPROPION HYDROCHLORIDE ()

Drug Information

Product NDC: 55648-105

Proprietary Name: Bupropion Hydrochloride

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Wockhardt Limited
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:8/30/2012

Package Information

No. Package Code Package Description Billing Unit
155648-105-0130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55648-105-01)
255648-105-0260 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55648-105-02)
355648-105-03100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55648-105-03)
455648-105-04500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55648-105-04)
555648-105-0510 BLISTER PACK in 1 CARTON (55648-105-05) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (55648-105-07)

NDC Record

Field Name Field Value Definition
PRODUCT NDC55648-105The 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 NAMEBupropion HydrochlorideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIX(SR)A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
START MARKETING DATE8/30/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEWockhardt LimitedName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023