68788-7103 NDC - DICLOFENAC SODIUM AND MISOPROSTOL ()

Drug Information

Product NDC: 68788-7103

Proprietary Name: Diclofenac Sodium and Misoprostol

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:	3/13/2018

No.	Package Code	Package Description	Billing Unit
1	68788-7103-3	30 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7103-3)	EA
2	68788-7103-6	6 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7103-6)	EA

Field Name	Field Value	Definition
PRODUCT NDC	68788-7103	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	Diclofenac Sodium and Misoprostol	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	3/13/2018	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