68788-0985 NDC - TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN ()

Drug Information

Product NDC: 68788-0985

Proprietary Name: Tramadol Hydrochloride and Acetaminophen

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	Preferred Pharmaceuticals, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	12/17/2009

No.	Package Code	Package Description
1	68788-0985-1	100 TABLET in 1 BOTTLE, DISPENSING (68788-0985-1)
2	68788-0985-2	20 TABLET in 1 BOTTLE, DISPENSING (68788-0985-2)
3	68788-0985-3	30 TABLET in 1 BOTTLE, DISPENSING (68788-0985-3)
4	68788-0985-4	40 TABLET in 1 BOTTLE, DISPENSING (68788-0985-4)
5	68788-0985-5	50 TABLET in 1 BOTTLE, DISPENSING (68788-0985-5)
6	68788-0985-6	60 TABLET in 1 BOTTLE, DISPENSING (68788-0985-6)
7	68788-0985-8	120 TABLET in 1 BOTTLE, DISPENSING (68788-0985-8)
8	68788-0985-9	90 TABLET in 1 BOTTLE, DISPENSING (68788-0985-9)

Field Name	Field Value	Definition
PRODUCT NDC	68788-0985	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	Tramadol Hydrochloride and 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	12/17/2009	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Preferred Pharmaceuticals, Inc.	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