25021-789 NDC - GLYCOPYRROLATE ()

Drug Information

Product NDC: 25021-789

Proprietary Name: Glycopyrrolate

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Sagent Pharmaceuticals
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:2/15/2022

Package Information

No. Package Code Package Description Billing Unit
125021-789-0110 VIAL in 1 CARTON (25021-789-01) / 1 mL in 1 VIAL
225021-789-0210 VIAL in 1 CARTON (25021-789-02) / 2 mL in 1 VIAL
325021-789-0510 VIAL in 1 CARTON (25021-789-05) / 5 mL in 1 VIAL

NDC Record

Field Name Field Value Definition
PRODUCT NDC25021-789The 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 NAMEGlycopyrrolateThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE2/15/2022This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESagent PharmaceuticalsName 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