42507-500 NDC - COUGH ()

Drug Information

No.	Package Code	Package Description	Billing Unit
1	42507-500-40	355 mL in 1 BOTTLE (42507-500-40)

Field Name	Field Value	Definition
PRODUCT NDC	42507-500	The translation of the dosage form Code submitted by the firm.
PROPRIETARY NAME	Cough	The translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE	2/12/2014	This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE	1/12/2019
MARKETING CATEGORY NAME	OTC MONOGRAPH FINAL	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.
APPLICATION NUMBER	part341	This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAME	HyVee Inc	Name of Company corresponding to the labeler code segment of the Product NDC.