61748-304 NDC - MYORISAN ()

Drug Information

Product NDC: 61748-304

Proprietary Name: Myorisan

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

No.	Package Code	Package Description	Billing Unit
1	61748-304-01	5000 CAPSULE, LIQUID FILLED in 1 BAG (61748-304-01)
2	61748-304-11	10 BLISTER PACK in 1 CARTON (61748-304-11) / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK	EA
3	61748-304-13	3 BLISTER PACK in 1 CARTON (61748-304-13) / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK	EA

Field Name	Field Value	Definition
PRODUCT NDC	61748-304	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	Myorisan	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	5/1/2012	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Akorn Operating Company LLC	Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 4/12/2024