0641-6033 NDC - GLYCOPYRROLATE ()

Drug Information

Product NDC: 0641-6033

Proprietary Name: Glycopyrrolate

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: West-ward Pharmaceutical Corp.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:2/6/1975

Package Information

No. Package Code Package Description Billing Unit
10641-6033-2525 VIAL in 1 CARTON (0641-6033-25) / 1 mL in 1 VIAL (0641-6033-01)ML

NDC Record

Field Name Field Value Definition
PRODUCT NDC0641-6033The 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 DATE2/6/1975This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEWest-ward Pharmaceutical Corp.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