0527-3220 NDC - DANTROLENE SODIUM ()

Drug Information

No.	Package Code	Package Description	Billing Unit
1	0527-3220-37	100 CAPSULE in 1 BOTTLE (0527-3220-37)	EA

Field Name	Field Value	Definition
PRODUCT NDC	0527-3220	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	Dantrolene Sodium	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	10/26/2005	This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE	10/1/2024	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
MARKETING CATEGORY NAME	ANDA	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
APPLICATION NUMBER	ANDA076686	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
LABELER NAME	Lannett Company, Inc.	The translation of the dosage form Code submitted by the firm.