17856-0201 NDC - CHILDRENS ACETAMINOPHEN ()

Drug Information

Product NDC: 17856-0201

Proprietary Name: Childrens Acetaminophen

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

No.	Package Code	Package Description
1	17856-0201-1	120 SYRINGE in 1 BOX, UNIT-DOSE (17856-0201-1) / 2.5 mL in 1 SYRINGE
2	17856-0201-2	120 SYRINGE in 1 BOX, UNIT-DOSE (17856-0201-2) / 1.25 mL in 1 SYRINGE
3	17856-0201-3	48 SYRINGE in 1 BOX, UNIT-DOSE (17856-0201-3) / 5 mL in 1 SYRINGE
4	17856-0201-4	72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0201-4) / 5 mL in 1 CUP, UNIT-DOSE
5	17856-0201-5	60 SYRINGE in 1 BOX, UNIT-DOSE (17856-0201-5) / 2.5 mL in 1 SYRINGE
6	17856-0201-6	48 SYRINGE in 1 BOX, UNIT-DOSE (17856-0201-6) / 7.5 mL in 1 SYRINGE
7	17856-0201-7	72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0201-7) / 15 mL in 1 CUP, UNIT-DOSE
8	17856-0201-8	120 SYRINGE in 1 BOX, UNIT-DOSE (17856-0201-8) / 2 mL in 1 SYRINGE
9	17856-0201-9	120 SYRINGE in 1 BOX, UNIT-DOSE (17856-0201-9) / 2.5 mL in 1 SYRINGE

Field Name	Field Value	Definition
PRODUCT NDC	17856-0201	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	Childrens Acetaminophen	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	4/9/2014	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