68387-170 NDC - METHYLPREDNISOLONE ()

Drug Information

Product NDC: 68387-170

Proprietary Name: Methylprednisolone

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Keltman Pharmaceuticals Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:9/14/2007

Package Information

No. Package Code Package Description Billing Unit
168387-170-011 DOSE PACK in 1 BAG (68387-170-01) / 21 TABLET in 1 DOSE PACKEA

NDC Record

Field Name Field Value Definition
PRODUCT NDC68387-170The 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 NAMEMethylprednisoloneThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE9/14/2007This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEKeltman Pharmaceuticals Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023