65977-5025 NDC - FINASTERIDE ()

Drug Information

Product NDC: 65977-5025

Proprietary Name: Finasteride

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

No.	Package Code	Package Description
1	65977-5025-0	48 BOTTLE in 1 CONTAINER (65977-5025-0) / 30 TABLET in 1 BOTTLE
2	65977-5025-1	48 BOTTLE in 1 CONTAINER (65977-5025-1) / 100 TABLET in 1 BOTTLE
3	65977-5025-2	48 BOTTLE in 1 CONTAINER (65977-5025-2) / 1000 TABLET in 1 BOTTLE
4	65977-5025-3	48 BOTTLE in 1 CONTAINER (65977-5025-3) / 90 TABLET in 1 BOTTLE
5	65977-5025-4	48 BOTTLE in 1 CONTAINER (65977-5025-4) / 500 TABLET in 1 BOTTLE

Field Name	Field Value	Definition
PRODUCT NDC	65977-5025	The 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 NAME	Finasteride	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	6/7/2010	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Hetero Drugs Limited	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