58118-0001 NDC - METHYLPREDNISOLONE ()

Drug Information

Field Name	Field Value
Labeler Name:	Clinical Solutions Wholesale
Product Type:
FDA Application Number:	ANDA040189
Marketing Category:	ANDA
Start Marketing Date:	10/31/1997
End Marketing Date:	6/15/2017

No.	Package Code	Package Description
1	58118-0001-0	1 TABLET in 1 PACKET (58118-0001-0)
2	58118-0001-2	21 TABLET in 1 BLISTER PACK (58118-0001-2)
3	58118-0001-3	30 TABLET in 1 BOTTLE, PLASTIC (58118-0001-3)
4	58118-0001-8	30 TABLET in 1 BLISTER PACK (58118-0001-8)

Field Name	Field Value	Definition
PRODUCT NDC	58118-0001	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	Methylprednisolone	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	10/31/1997	This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE	6/15/2017	This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
MARKETING CATEGORY NAME	ANDA	Name of Company corresponding to the labeler code segment of the Product NDC.
APPLICATION NUMBER	ANDA040189	Name of Company corresponding to the labeler code segment of the Product NDC.
LABELER NAME	Clinical Solutions Wholesale	Name of Company corresponding to the labeler code segment of the Product NDC.