0998-0630 NDC - MAXITROL ()

Drug Information

Product NDC: 0998-0630

Proprietary Name: Maxitrol

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Alcon Laboratories, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:11/15/1964

Package Information

No. Package Code Package Description Billing Unit
10998-0630-065 mL in 1 BOTTLE, PLASTIC (0998-0630-06)ML

NDC Record

Field Name Field Value Definition
PRODUCT NDC0998-0630The 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 NAMEMaxitrolThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE11/15/1964This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEAlcon Laboratories, 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