54868-0065 NDC - AMITRIPTYLINE HYDROCHLORIDE ()

Drug Information

Product NDC: 54868-0065

Proprietary Name: Amitriptyline 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:11/7/1995

Package Information

No. Package Code Package Description Billing Unit
154868-0065-01000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-0065-0)EA
254868-0065-230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-0065-2)EA
354868-0065-360 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-0065-3)EA
454868-0065-420 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-0065-4)EA
554868-0065-550 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-0065-5)EA
654868-0065-790 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-0065-7)
754868-0065-8100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-0065-8)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC54868-0065The 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 NAMEAmitriptyline 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 DATE11/7/1995This 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