65483-991 NDC - ZYLOPRIM ()

Drug Information

Product NDC: 65483-991

Proprietary Name: ZYLOPRIM

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

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

No.	Package Code	Package Description	Billing Unit
1	65483-991-10	100 TABLET in 1 BOTTLE (65483-991-10)	EA

Field Name	Field Value	Definition
PRODUCT NDC	65483-991	The 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 NAME	ZYLOPRIM	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	8/19/1966	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Prometheus 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: 2/1/2023