Skip to the page

Data / Drug companies / Dr. Reddy's Laboratories Inc.

Dr. Reddy's Laboratories Inc.: 9 products in the FDA NDC directory, labeler code 55741

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

Dr. Reddy's Laboratories Inc. (labeler code 55741) lists 9 products in the FDA National Drug Code Directory, covering 5 finished drugs by generic name. By type: 8 over the counter drugs, 1 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on February 13, 2026.

The request: Watch Dr. Reddy's Laboratories Inc. (FDA labeler code 55741): 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
55741
Products in commercial distribution
9
Packages
20
Finished drugs by generic name
5
Prescription products
1
Over the counter products
8
Flagged as original packager
9 of 9 products that carry the flag
Started marketing in the last 12 months
1
Earliest marketing start
May 14, 2015
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
New drug applications (NDA)444.4%
Generic drugs (ANDA)333.3%
Over the counter monograph drugs222.2%

Products by type

TypeProductsShare
Over the counter drugs888.9%
Prescription drugs111.1%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Patch, extended release333.3%
Tablet222.2%
Gum, chewing222.2%
Kit222.2%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Lutera55741-005KitGeneric drugs (ANDA)February 13, 2026
Habitrol Nicotine Polacrilex 2 mg Coated Cinnamon55741-004Gum, chewingGeneric drugs (ANDA)July 28, 2025
Habitrol Nicotine Polacrilex 4 mg Coated Cinnamon55741-001Gum, chewingGeneric drugs (ANDA)July 28, 2025
Habitrol Step 155741-448Patch, extended releaseNew drug applications (NDA)July 13, 2018
Habitrol Step 255741-447Patch, extended releaseNew drug applications (NDA)July 13, 2018
Habitrol Step 355741-446Patch, extended releaseNew drug applications (NDA)July 13, 2018
Doans Maximum Strength55741-600TabletOver the counter monograph drugsMay 24, 2016
Doans Extra Strength55741-224TabletOver the counter monograph drugsMay 24, 2016
Nicotine transdermal system55741-449KitNew drug applications (NDA)May 14, 2015

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.