68387-100 NDC - PROPOXYPHENE AND ACETAMINOPHEN ()

Drug Information

Product NDC: 68387-100

Proprietary Name: Propoxyphene and Acetaminophen

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	Keltman Pharmaceuticals Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	3/1/2009

No.	Package Code	Package Description
1	68387-100-10	10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68387-100-10)
2	68387-100-12	120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68387-100-12)
3	68387-100-15	15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68387-100-15)
4	68387-100-30	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68387-100-30)
5	68387-100-40	40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68387-100-40)
6	68387-100-50	50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68387-100-50)
7	68387-100-60	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68387-100-60)
8	68387-100-90	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68387-100-90)

Field Name	Field Value	Definition
PRODUCT NDC	68387-100	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	Propoxyphene 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	3/1/2009	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Keltman 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