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16590-620 NDC - PERCOCET ()

Drug Information

Product NDC: 16590-620

Proprietary Name: PERCOCET

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: STAT RX USA LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:7/30/1999

Package Information

No. Package Code Package Description Billing Unit
116590-620-3030 TABLET in 1 BOTTLE (16590-620-30)EA
216590-620-5656 TABLET in 1 BOTTLE (16590-620-56)EA
316590-620-6060 TABLET in 1 BOTTLE (16590-620-60)EA
416590-620-6284 TABLET in 1 BOTTLE (16590-620-62)EA
516590-620-72120 TABLET in 1 BOTTLE (16590-620-72)EA
616590-620-73112 TABLET in 1 BOTTLE (16590-620-73)EA
716590-620-82180 TABLET in 1 BOTTLE (16590-620-82)
816590-620-83150 TABLET in 1 BOTTLE (16590-620-83)EA
916590-620-9090 TABLET in 1 BOTTLE (16590-620-90)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC16590-620The 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 NAMEPERCOCETThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE7/30/1999This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESTAT RX USA LLCName 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