65044-7133 NDC - SODIUM CHLORIDE ()

Drug Information

Field Name	Field Value
Labeler Name:	Jubilant HollisterStier LLC
Product Type:
FDA Application Number:	ANDA203352
Marketing Category:	ANDA
Start Marketing Date:	2/29/2016
End Marketing Date:	6/30/2021

No.	Package Code	Package Description	Billing Unit
1	65044-7133-2	25 VIAL, GLASS in 1 CARTON (65044-7133-2) / 10 mL in 1 VIAL, GLASS (65044-7133-1)

Field Name	Field Value	Definition
PRODUCT NDC	65044-7133	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	sodium chloride	Name of Company corresponding to the labeler code segment of the Product NDC.
START MARKETING DATE	2/29/2016	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.
END MARKETING DATE	6/30/2021
MARKETING CATEGORY NAME	ANDA
APPLICATION NUMBER	ANDA203352	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	Jubilant HollisterStier LLC	Name of Company corresponding to the labeler code segment of the Product NDC.