0069-3080 NDC - ZITHROMAX ()

Drug Information

Field Name	Field Value
Labeler Name:	Pfizer Laboratories Div Pfizer Inc
Product Type:
FDA Application Number:	NDA050730
Marketing Category:	NDA
Start Marketing Date:	6/12/1996
End Marketing Date:	9/30/2018

No.	Package Code	Package Description	Billing Unit
1	0069-3080-30	30 TABLET, FILM COATED in 1 BOTTLE (0069-3080-30)	EA

Field Name	Field Value	Definition
PRODUCT NDC	0069-3080	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	ZITHROMAX	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	6/12/1996	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
END MARKETING DATE	9/30/2018	The translation of the dosage form Code submitted by the firm.
MARKETING CATEGORY NAME	NDA	The translation of the route code submitted by the firm, indicating route of administration.
APPLICATION NUMBER	NDA050730	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Pfizer Laboratories Div Pfizer Inc	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.