54868-0699 NDC - SPIRONOLACTONE AND HYDROCHLOROTHIAZIDE ()

Drug Information

Product NDC: 54868-0699

Proprietary Name: Spironolactone and Hydrochlorothiazide

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:5/26/1993

Package Information

No. Package Code Package Description Billing Unit
154868-0699-1100 TABLET in 1 BOTTLE, PLASTIC (54868-0699-1)EA
254868-0699-230 TABLET in 1 BOTTLE, PLASTIC (54868-0699-2)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC54868-0699The 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 NAMESpironolactone and HydrochlorothiazideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/26/1993This 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