68554-3026 NDC - FINASTERIDE ()

Drug Information

Product NDC: 68554-3026

Proprietary Name: Finasteride

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Hetero Labs Limited
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:7/1/2013

Package Information

No. Package Code Package Description Billing Unit
168554-3026-030 TABLET, FILM COATED in 1 BOTTLE (68554-3026-0)
268554-3026-190 TABLET, FILM COATED in 1 BOTTLE (68554-3026-1)
368554-3026-21000 TABLET, FILM COATED in 1 BOTTLE (68554-3026-2)

NDC Record

Field Name Field Value Definition
PRODUCT NDC68554-3026The 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 NAMEFinasterideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE7/1/2013This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEHetero Labs LimitedName 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