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Data / Drug companies / Sun Pharmaceutical Industries, Inc.

Sun Pharmaceutical Industries, Inc.: 16 products in the FDA NDC directory, labeler code 10631

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

Sun Pharmaceutical Industries, Inc. (labeler code 10631) lists 16 products in the FDA National Drug Code Directory, covering 4 finished drugs by generic name. By type: 16 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on November 20, 2019.

The request: Watch Sun Pharmaceutical Industries, Inc. (FDA labeler code 10631): 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
10631
Products in commercial distribution
16
Packages
19
Finished drugs by generic name
4
Prescription products
16
Over the counter products
0
Flagged as original packager
15 of 15 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
April 28, 2005
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)1593.8%
Generic drugs (ANDA)16.2%

Products by type

TypeProductsShare
Prescription drugs16100%

Drugs it lists

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

DrugProductsCompanies listing it
Isotretinoin1016
Metoprolol succinate446
Hydrocortisone1171
Halcinonide cream12

Dosage forms

Dosage formProductsShare
Capsule1062.5%
Capsule, extended release425%
Cream212.5%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Absorica LD10631-007CapsuleNew drug applications (NDA)November 20, 2019
Absorica LD10631-005CapsuleNew drug applications (NDA)November 20, 2019
Absorica LD10631-003CapsuleNew drug applications (NDA)November 20, 2019
Absorica LD10631-002CapsuleNew drug applications (NDA)November 20, 2019
Kapspargo10631-011Capsule, extended releaseNew drug applications (NDA)March 15, 2018
Kapspargo10631-010Capsule, extended releaseNew drug applications (NDA)March 15, 2018
Kapspargo10631-009Capsule, extended releaseNew drug applications (NDA)March 15, 2018
Kapspargo10631-008Capsule, extended releaseNew drug applications (NDA)March 15, 2018
Absorica10631-134CapsuleNew drug applications (NDA)February 17, 2015
Absorica10631-133CapsuleNew drug applications (NDA)February 17, 2015
Absorica10631-118CapsuleNew drug applications (NDA)June 8, 2012
Absorica10631-117CapsuleNew drug applications (NDA)June 8, 2012
Absorica10631-116CapsuleNew drug applications (NDA)June 8, 2012
Absorica10631-115CapsuleNew drug applications (NDA)June 8, 2012
Halog10631-094CreamNew drug applications (NDA)February 10, 2009
Proctosol-HC10631-407CreamGeneric drugs (ANDA)April 28, 2005

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.