49999-349 NDC - BUPROPION HYDROCHLORIDE ()

Drug Information

Product NDC: 49999-349

Proprietary Name: Bupropion Hydrochloride

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:2/7/2000

Package Information

No. Package Code Package Description Billing Unit
149999-349-3060 TABLET, FILM COATED in 1 BOTTLE (49999-349-30)EA
249999-349-6030 TABLET, FILM COATED in 1 BOTTLE (49999-349-60)EA
349999-349-9090 TABLET, FILM COATED in 1 BOTTLE (49999-349-90)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC49999-349The 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.
START MARKETING DATE2/7/2000This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMELake Erie Medical DBA Quality Care Products LLCName 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