54868-0122 NDC - TRAZODONE HYDROCHLORIDE ()

Drug Information

Product NDC: 54868-0122

Proprietary Name: Trazodone Hydrochloride

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:4/9/1996

Package Information

No. Package Code Package Description Billing Unit
154868-0122-0100 TABLET in 1 BOTTLE (54868-0122-0)EA
254868-0122-230 TABLET in 1 BOTTLE (54868-0122-2)EA
354868-0122-360 TABLET in 1 BOTTLE (54868-0122-3)EA
454868-0122-590 TABLET in 1 BOTTLE (54868-0122-5)EA
554868-0122-6100 TABLET in 1 BOTTLE, UNIT-DOSE (54868-0122-6)EA
654868-0122-720 TABLET in 1 BOTTLE (54868-0122-7)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC54868-0122The 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 NAMETrazodone 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 DATE4/9/1996This 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