58607-112 NDC - MYFERON 150 FORTE ()

Drug Information

Product NDC: 58607-112

Proprietary Name: Myferon 150 Forte

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: MARTIN EKWEALOR PHARMACEUTICALS, INC.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:12/1/1996

Package Information

No. Package Code Package Description Billing Unit
158607-112-00100 BLISTER PACK in 1 BOX (58607-112-00) / 10 CAPSULE in 1 BLISTER PACKEA

NDC Record

Field Name Field Value Definition
PRODUCT NDC58607-112The 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 NAMEMyferon 150 ForteThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE12/1/1996This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEMARTIN EKWEALOR 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