54868-4976 NDC - HYDROCODONE BITARTRATE AND IBUPROFEN ()

Drug Information

Product NDC: 54868-4976

Proprietary Name: HYDROCODONE BITARTRATE AND IBUPROFEN

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Physicians Total Care, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:7/25/2005

Package Information

No. Package Code Package Description Billing Unit
154868-4976-030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-4976-0)EA
254868-4976-120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-4976-1)EA
354868-4976-2120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-4976-2)EA
454868-4976-340 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-4976-3)EA
554868-4976-4100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-4976-4)EA
654868-4976-560 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-4976-5)EA
754868-4976-6180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-4976-6)EA
854868-4976-790 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-4976-7)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC54868-4976The 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 NAMEHYDROCODONE BITARTRATE AND IBUPROFENThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE7/25/2005This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEPhysicians Total Care, Inc.Name 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