68982-820 NDC - PANZYGA ()

Drug Information

Product NDC: 68982-820

Proprietary Name: Panzyga

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Octapharma USA Inc
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:11/12/2018

Package Information

No. Package Code Package Description Billing Unit
168982-820-011 BOTTLE, GLASS in 1 CARTON (68982-820-01) / 10 mL in 1 BOTTLE, GLASS (68982-820-81)ML
268982-820-021 BOTTLE, GLASS in 1 CARTON (68982-820-02) / 25 mL in 1 BOTTLE, GLASS (68982-820-82)ML
368982-820-031 BOTTLE, GLASS in 1 CARTON (68982-820-03) / 50 mL in 1 BOTTLE, GLASS (68982-820-83)ML
468982-820-041 BOTTLE, GLASS in 1 CARTON (68982-820-04) / 100 mL in 1 BOTTLE, GLASS (68982-820-84)ML
568982-820-051 BOTTLE, GLASS in 1 CARTON (68982-820-05) / 200 mL in 1 BOTTLE, GLASS (68982-820-85)ML
668982-820-061 BOTTLE, GLASS in 1 CARTON (68982-820-06) / 300 mL in 1 BOTTLE, GLASS (68982-820-86)ML

NDC Record

Field Name Field Value Definition
PRODUCT NDC68982-820The 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 NAMEPanzygaThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE11/12/2018This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEOctapharma USA IncName 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