12634-179 NDC - METHERGINE ()

Drug Information

Product NDC: 12634-179

Proprietary Name: METHERGINE

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Apotheca, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:12/27/2006

Package Information

No. Package Code Package Description Billing Unit
112634-179-0010 TABLET, COATED in 1 BOTTLE, PLASTIC (12634-179-00)
212634-179-8020 TABLET, COATED in 1 BOTTLE, PLASTIC (12634-179-80)
312634-179-8212 TABLET, COATED in 1 BOTTLE, PLASTIC (12634-179-82)
412634-179-8515 TABLET, COATED in 1 BOTTLE, PLASTIC (12634-179-85)
512634-179-911 TABLET, COATED in 1 BLISTER PACK (12634-179-91)
612634-179-966 TABLET, COATED in 1 BOTTLE, PLASTIC (12634-179-96)
712634-179-988 TABLET, COATED in 1 BOTTLE, PLASTIC (12634-179-98)

NDC Record

Field Name Field Value Definition
PRODUCT NDC12634-179The 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 NAMEMETHERGINEThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE12/27/2006This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEApotheca, 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