80637-001 NDC - C-TIZERS 99.9 ()

Drug Information

Product NDC: 80637-001

Proprietary Name: C-tizers 99.9

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: TIZER KOZMETIK LIMITED SIRKETI
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:10/6/2020

Package Information

No. Package Code Package Description Billing Unit
180637-001-011.5 mL in 1 POUCH (80637-001-01)
280637-001-021.5 mL in 1 PACKET (80637-001-02)
380637-001-033 mL in 1 POUCH (80637-001-03)
480637-001-043 mL in 1 PACKET (80637-001-04)
580637-001-0550 mL in 1 BOTTLE (80637-001-05)
680637-001-06100 mL in 1 BOTTLE (80637-001-06)
780637-001-07250 mL in 1 BOTTLE (80637-001-07)
880637-001-08500 mL in 1 BOTTLE (80637-001-08)
980637-001-091000 mL in 1 BOTTLE (80637-001-09)
1080637-001-105000 mL in 1 BOTTLE (80637-001-10)
1180637-001-11150000 mL in 1 DRUM (80637-001-11)
1280637-001-1245 mL in 1 POUCH (80637-001-12)

NDC Record

Field Name Field Value Definition
PRODUCT NDC80637-001The 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 NAMEC-tizers 99.9The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE10/6/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMETIZER KOZMETIK LIMITED SIRKETIName 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