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Data / Drug companies / Sun Pharmaceutical Industries, Inc.

Sun Pharmaceutical Industries, Inc.: 24 products in the FDA NDC directory, labeler code 70095

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

Sun Pharmaceutical Industries, Inc. (labeler code 70095) lists 24 products in the FDA National Drug Code Directory, covering 12 finished drugs by generic name. By type: 20 prescription drugs, 4 bulk ingredients. Its main marketing category is generic drugs (ANDA). The newest product started marketing on August 31, 2026.

The request: Watch Sun Pharmaceutical Industries, Inc. (FDA labeler code 70095): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
70095
Products in commercial distribution
24
Packages
31
Finished drugs by generic name
12
Prescription products
20
Over the counter products
0
Flagged as original packager
11 of 11 products that carry the flag
Started marketing in the last 12 months
12
Earliest marketing start
March 27, 2023
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)1875%
Bulk ingredients416.7%
Biologics (BLA)14.2%
Authorized generics (NDA)14.2%

Products by type

TypeProductsShare
Prescription drugs2083.3%
Bulk ingredients416.7%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Capsule416.7%
Injection, solution416.7%
Tablet416.7%
Powder416.7%
Injection, powder, lyophilized, for solution28.3%
Tablet, film coated28.3%
Insert14.2%
Solution14.2%
Injection14.2%
Injection, emulsion14.2%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Pomalidomide70095-060CapsuleGeneric drugs (ANDA)August 31, 2026
Pomalidomide70095-059CapsuleGeneric drugs (ANDA)August 31, 2026
Pomalidomide70095-058CapsuleGeneric drugs (ANDA)August 31, 2026
Pomalidomide70095-057CapsuleGeneric drugs (ANDA)August 31, 2026
Methylnaltrexone bromide70095-218PowderBulk ingredientsJune 10, 2026
Phytonadione70095-154Injection, emulsionGeneric drugs (ANDA)June 10, 2026
Tofacitinib70095-008SolutionGeneric drugs (ANDA)June 3, 2026
Istradefylline70095-214PowderBulk ingredientsMay 25, 2026
Vismodegib70095-210PowderBulk ingredientsMay 25, 2026
Progesterone70095-136InsertAuthorized generics (NDA)April 27, 2026
Sincalide70095-212PowderBulk ingredientsApril 16, 2026
Unloxcyt70095-130Injection, solutionBiologics (BLA)December 8, 2025
Eribulin mesylate70095-080InjectionGeneric drugs (ANDA)May 15, 2025
Deflazacort70095-043TabletGeneric drugs (ANDA)March 19, 2025
Deflazacort70095-042TabletGeneric drugs (ANDA)March 19, 2025
Deflazacort70095-041TabletGeneric drugs (ANDA)March 19, 2025
Deflazacort70095-040TabletGeneric drugs (ANDA)March 19, 2025
Sodium bicarbonate70095-050Injection, solutionGeneric drugs (ANDA)March 15, 2024
Bisoprolol fumarate70095-020Tablet, film coatedGeneric drugs (ANDA)March 10, 2024
Bisoprolol fumarate70095-019Tablet, film coatedGeneric drugs (ANDA)March 10, 2024
Desmopressin Acetate70095-031Injection, solutionGeneric drugs (ANDA)June 20, 2023
Desmopressin Acetate70095-026Injection, solutionGeneric drugs (ANDA)April 3, 2023
Pantoprazole sodium70095-024Injection, powder, lyophilized, for solutionGeneric drugs (ANDA)April 3, 2023
Azithromycin monohydrate70095-025Injection, powder, lyophilized, for solutionGeneric drugs (ANDA)March 27, 2023

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.