17856-5401 NDC - ACETAMINOPHEN ()

Drug Information

Product NDC: 17856-5401

Proprietary Name: ACETAMINOPHEN

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: ATLANTIC BIOLOGICALS CORP.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:7/28/2020

Package Information

No. Package Code Package Description Billing Unit
117856-5401-1120 SYRINGE in 1 BOX, UNIT-DOSE (17856-5401-1) / 1.5 mL in 1 SYRINGE
217856-5401-2120 SYRINGE in 1 BOX, UNIT-DOSE (17856-5401-2) / 2 mL in 1 SYRINGE
317856-5401-3120 SYRINGE in 1 BOX, UNIT-DOSE (17856-5401-3) / 3 mL in 1 SYRINGE
417856-5401-448 SYRINGE in 1 BOX, UNIT-DOSE (17856-5401-4) / 3.75 mL in 1 SYRINGE
517856-5401-572 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-5401-5) / 5 mL in 1 CUP, UNIT-DOSE
617856-5401-648 SYRINGE in 1 BOX, UNIT-DOSE (17856-5401-6) / 6 mL in 1 SYRINGE
717856-5401-748 SYRINGE in 1 BOX, UNIT-DOSE (17856-5401-7) / 7.5 mL in 1 SYRINGE
817856-5401-872 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-5401-8) / 10.15 mL in 1 CUP, UNIT-DOSE
917856-5401-950 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-5401-9) / 15 mL in 1 CUP, UNIT-DOSE

NDC Record

Field Name Field Value Definition
PRODUCT NDC17856-5401The 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 NAMEACETAMINOPHENThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE7/28/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEATLANTIC 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