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Data / Drug companies / Marc Glassman, Inc.

Marc Glassman, Inc.: 64 products in the FDA NDC directory, labeler code 68998

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Marc Glassman, Inc. (labeler code 68998) lists 64 products in the FDA National Drug Code Directory, covering 30 finished drugs by generic name. By type: 64 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on August 29, 2025.

The request: Watch Marc Glassman, Inc. (FDA labeler code 68998): each new product listing and each discontinued product. $10 of work on sign-up, no card.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Labeler code
68998
Products in commercial distribution
64
Packages
73
Finished drugs by generic name
30
Prescription products
0
Over the counter products
64
Flagged as original packager
59 of 59 products that carry the flag
Started marketing in the last 12 months
0
Products with a marketing end date set
1
Earliest marketing start
March 25, 2002
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Over the counter monograph drugs4875%
Generic drugs (ANDA)1625%

Products by type

TypeProductsShare
Over the counter drugs64100%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

Dosage forms

Dosage formProductsShare
Tablet, coated2843.8%
Tablet812.5%
Tablet, chewable57.8%
Capsule46.2%
Mouthwash34.7%
Tablet, delayed release34.7%
Shampoo34.7%
Suspension23.1%
Liquid23.1%
Capsule, liquid filled11.6%
Enema11.6%
Spray11.6%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Allergy Relief Nasal68998-452Spray, meteredGeneric drugs (ANDA)August 29, 2025
8 Hour Arthritis Pain68998-401Tablet, extended releaseGeneric drugs (ANDA)October 5, 2022
Pain Relief Extra Strength68998-392Tablet, coatedOver the counter monograph drugsOctober 5, 2022
Pain Relief Regular Strength68998-301TabletOver the counter monograph drugsOctober 5, 2022
Cold plus Head Congestion Severe68998-275Tablet, coatedOver the counter monograph drugsOctober 5, 2022
Cold plus Flu Severe68998-263Tablet, coatedOver the counter monograph drugsOctober 5, 2022
Cold Max68998-238Tablet, coatedOver the counter monograph drugsOctober 5, 2022
Sinus Severe68998-219Tablet, coatedOver the counter monograph drugsOctober 5, 2022
Pain Relief Extra Strength68998-198Tablet, coatedOver the counter monograph drugsOctober 5, 2022
Pain Relief PM Extra Strength68998-195Tablet, coatedOver the counter monograph drugsOctober 5, 2022
Pain Relief Extra Strength68998-104Tablet, coatedOver the counter monograph drugsOctober 5, 2022
Pain Relief PM Extra Strength68998-071Tablet, coatedOver the counter monograph drugsSeptember 15, 2022
Pain Relief Extra Strength68998-070Tablet, coatedOver the counter monograph drugsSeptember 15, 2022
Chewable Aspirin68998-205Tablet, chewableOver the counter monograph drugsAugust 31, 2021
Allergy Relief68998-292TabletGeneric drugs (ANDA)July 9, 2021
Stomach Relief, Ultra Strength68998-558SuspensionOver the counter monograph drugsDecember 15, 2020
Allergy Multi Symptom68998-228Tablet, coatedOver the counter monograph drugsJune 22, 2020
Sinus Pressure plus Pain PE68998-220Tablet, coatedOver the counter monograph drugsJune 22, 2020
Sinus plus Headache68998-323Tablet, coatedOver the counter monograph drugsJune 15, 2020
Allergy Relief68998-414TabletGeneric drugs (ANDA)May 1, 2020
Ibuprofen68998-011Tablet, coatedGeneric drugs (ANDA)May 1, 2020
Childrens Ibuprofen Oral Suspension68998-320SuspensionGeneric drugs (ANDA)March 9, 2020
Allergy Relief68998-194Tablet, coatedGeneric drugs (ANDA)March 1, 2020
Ibuprofen68998-012Tablet, coatedGeneric drugs (ANDA)March 1, 2020
Marcs Mucus Relief68998-845TabletOver the counter monograph drugsFebruary 26, 2020

CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.