51862-510 NDC - TRIVORA ()

Drug Information

No.	Package Code	Package Description	Billing Unit
1	51862-510-06	6 BLISTER PACK in 1 CARTON (51862-510-06) / 1 KIT in 1 BLISTER PACK (51862-510-01)	EA

Field Name	Field Value	Definition
PRODUCT NDC	51862-510	This is the date that the labeler indicates was the start of its marketing of the drug product.
PROPRIETARY NAME	Trivora	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.
START MARKETING DATE	8/3/2016	This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE	6/30/2025	Name of Company corresponding to the labeler code segment of the Product NDC.
MARKETING CATEGORY NAME	ANDA	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
APPLICATION NUMBER	ANDA074538
LABELER NAME	Mayne Pharma Inc.