44911-0174 NDC - RHEUMATISM ()

Drug Information

No.	Package Code	Package Description	Billing Unit
1	44911-0174-1	30 mL in 1 BOTTLE, DROPPER (44911-0174-1)

Field Name	Field Value	Definition
PRODUCT NDC	44911-0174	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	Rheumatism	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIX	HP	A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
START MARKETING DATE	7/7/2015	This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE	9/23/2024	The translation of the dosage form Code submitted by the firm.
MARKETING CATEGORY NAME	UNAPPROVED HOMEOPATHIC	The translation of the route code submitted by the firm, indicating route of administration.
LABELER NAME	Energique, Inc.	This is the date that the labeler indicates was the start of its marketing of the drug product.