17856-0962 NDC - POLYETHYLENE GLYCOL 3350 ()

Drug Information

Product NDC: 17856-0962

Proprietary Name: Polyethylene Glycol 3350

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

No.	Package Code	Package Description	Billing Unit
1	17856-0962-1	72 POUCH in 1 BOX, UNIT-DOSE (17856-0962-1) / 4 g in 1 POUCH	EA
2	17856-0962-2	72 POUCH in 1 BOX, UNIT-DOSE (17856-0962-2) / 4.25 g in 1 POUCH	EA
3	17856-0962-3	50 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0962-3) / 8.5 g in 1 CUP, UNIT-DOSE	EA
4	17856-0962-4	72 POUCH in 1 BOX, UNIT-DOSE (17856-0962-4) / 8.5 g in 1 POUCH	EA
5	17856-0962-5	50 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0962-5) / 4.25 g in 1 CUP, UNIT-DOSE

Field Name	Field Value	Definition
PRODUCT NDC	17856-0962	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	Polyethylene Glycol 3350	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	3/27/2019	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	ATLANTIC BIOLOGICALS CORP.	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