48083-310 NDC - CERTI-CET PLUS ()

Drug Information

Product NDC: 48083-310

Proprietary Name: CERTI-CET PLUS

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Certified Safety Manufacturing
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:12/29/2017

Package Information

No. Package Code Package Description Billing Unit
148083-310-2725 POUCH in 1 BOX (48083-310-27) / 2 TABLET in 1 POUCH
248083-310-3050 POUCH in 1 BOX (48083-310-30) / 2 TABLET in 1 POUCH
348083-310-3150 POUCH in 1 BOX (48083-310-31) / 2 TABLET in 1 POUCH
448083-310-33125 POUCH in 1 BOX (48083-310-33) / 2 TABLET in 1 POUCH
548083-310-36250 POUCH in 1 BOX (48083-310-36) / 2 TABLET in 1 POUCH
648083-310-39500 POUCH in 1 BOX (48083-310-39) / 2 TABLET in 1 POUCH

NDC Record

Field Name Field Value Definition
PRODUCT NDC48083-310The 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 NAMECERTI-CET PLUSThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXExtra StrengthA suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
START MARKETING DATE12/29/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMECertified Safety ManufacturingName 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