53808-0795 NDC - ZERIT ()

Drug Information

Product NDC: 53808-0795

Proprietary Name: ZERIT

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: State of Florida DOH Central Pharmacy
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:7/1/2009

Package Information

No. Package Code Package Description Billing Unit
153808-0795-130 CAPSULE, GELATIN COATED in 1 BLISTER PACK (53808-0795-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC53808-0795The 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 NAMEZERITThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE7/1/2009This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEState of Florida DOH Central PharmacyName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/19/2021