Data / Drug companies / Glenmark Therapeutics Inc., USA

Glenmark Therapeutics Inc., USA: 23 products in the FDA NDC directory, labeler code 72657

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

Glenmark Therapeutics Inc., USA (labeler code 72657) lists 23 products in the FDA National Drug Code Directory, covering 12 finished drugs by generic name. By type: 23 over the counter drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on November 1, 2026.

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Labeler code

72657

Products in commercial distribution

23

Packages

77

Finished drugs by generic name

12

Prescription products

0

Over the counter products

23

Flagged as original packager

19 of 19 products that carry the flag

Started marketing in the last 12 months

6

Earliest marketing start

June 1, 2022

openFDA record search

api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Products by type

Drugs it lists

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

Dosage forms

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

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.