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0440-7200 NDC - BUPROPION HYDROCHLORIDE ()

Drug Information

Product NDC: 0440-7200

Proprietary Name: Bupropion Hydrochloride

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Liberty Pharmaceuticals, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/12/2008

Package Information

No. Package Code Package Description Billing Unit
10440-7200-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0440-7200-30)
20440-7200-6060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0440-7200-60)
30440-7200-81300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0440-7200-81)
40440-7200-9090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0440-7200-90)
50440-7200-91120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0440-7200-91)
60440-7200-92180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0440-7200-92)

NDC Record

Field Name Field Value Definition
PRODUCT NDC0440-7200The 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 DATE3/12/2008This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMELiberty Pharmaceuticals, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 11/10/2022