65483-993 NDC - ZYLOPRIM ()

Drug Information

Product NDC: 65483-993

Proprietary Name: ZYLOPRIM

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Prometheus Laboratories Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:8/19/1966

Package Information

No. Package Code Package Description Billing Unit
165483-993-10100 TABLET in 1 BOTTLE (65483-993-10)EA
265483-993-50500 TABLET in 1 BOTTLE (65483-993-50)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC65483-993The 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 NAMEZYLOPRIMThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/19/1966This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEPrometheus Laboratories Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 1/24/2020