54868-4984 NDC - LEVITRA ()

Drug Information

Product NDC: 54868-4984

Proprietary Name: Levitra

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:3/5/2004

Package Information

No. Package Code Package Description Billing Unit
154868-4984-05 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-4984-0)EA
254868-4984-13 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-4984-1)EA
354868-4984-24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-4984-2)EA
454868-4984-310 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-4984-3)EA
554868-4984-430 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-4984-4)
654868-4984-56 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-4984-5)

NDC Record

Field Name Field Value Definition
PRODUCT NDC54868-4984The 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 NAMELevitraThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/5/2004This 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