67777-306 NDC - DYNAREX HP 3 ()

Drug Information

Product NDC: 67777-306

Proprietary Name: Dynarex HP 3

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Dynarex Corporation
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/29/2014

Package Information

No. Package Code Package Description Billing Unit
167777-306-01118 mL in 1 BOTTLE (67777-306-01)
267777-306-02454 mL in 1 BOTTLE (67777-306-02)

NDC Record

Field Name Field Value Definition
PRODUCT NDC67777-306The 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 NAMEDynarex HP 3The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/29/2014This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEDynarex CorporationName 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