68788-9906 NDC - NAPROXEN ()

Drug Information

Product NDC: 68788-9906

Proprietary Name: Naproxen

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Preferred Pharmaceuticals, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/30/2012

Package Information

No. Package Code Package Description Billing Unit
168788-9906-1100 TABLET in 1 BOTTLE (68788-9906-1)
268788-9906-220 TABLET in 1 BOTTLE (68788-9906-2)
368788-9906-330 TABLET in 1 BOTTLE (68788-9906-3)
468788-9906-660 TABLET in 1 BOTTLE (68788-9906-6)
568788-9906-8120 TABLET in 1 BOTTLE (68788-9906-8)
668788-9906-990 TABLET in 1 BOTTLE (68788-9906-9)

NDC Record

Field Name Field Value Definition
PRODUCT NDC68788-9906The 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 NAMENaproxenThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/30/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEPreferred 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: 7/26/2021