Data / Drug companies / Sun Pharmaceutical Industries, Inc.
Sun Pharmaceutical Industries, Inc.: 76 products in the FDA NDC directory, labeler code 57664
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Sun Pharmaceutical Industries, Inc. (labeler code 57664) lists 76 products in the FDA National Drug Code Directory, covering 19 finished drugs by generic name. By type: 76 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on February 2, 2026.
The request: Watch Sun Pharmaceutical Industries, Inc. (FDA labeler code 57664): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 57664
- Products in commercial distribution
- 76
- Packages
- 119
- Finished drugs by generic name
- 19
- Prescription products
- 76
- Over the counter products
- 0
- Controlled substance products
- Schedule II 33
- Flagged as original packager
- 72 of 72 products that carry the flag
- Started marketing in the last 12 months
- 1
- Products with a marketing end date set
- 2
- Earliest marketing start
- July 14, 1987
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 69 | 90.8% |
| Authorized generics (NDA) | 7 | 9.2% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 76 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 32 | 42.1% |
| Capsule | 16 | 21.1% |
| Capsule, extended release | 8 | 10.5% |
| Tablet, film coated | 8 | 10.5% |
| Tablet, chewable | 6 | 7.9% |
| Injection, solution | 3 | 3.9% |
| Suspension | 1 | 1.3% |
| Tablet, extended release | 1 | 1.3% |
| Cream | 1 | 1.3% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Deflazacort Oral Suspension | 57664-993 | Suspension | Generic drugs (ANDA) | February 2, 2026 |
| Methylphenidate Hydrochloride | 57664-710 | Tablet, extended release | Generic drugs (ANDA) | December 20, 2024 |
| Levorphanol Tartrate | 57664-058 | Tablet | Generic drugs (ANDA) | June 15, 2024 |
| Dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate, amphetamine sulfate | 57664-953 | Capsule, extended release | Generic drugs (ANDA) | February 1, 2024 |
| Dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate, amphetamine sulfate | 57664-952 | Capsule, extended release | Generic drugs (ANDA) | February 1, 2024 |
| Dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate, amphetamine sulfate | 57664-951 | Capsule, extended release | Generic drugs (ANDA) | February 1, 2024 |
| Dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate, amphetamine sulfate | 57664-950 | Capsule, extended release | Generic drugs (ANDA) | February 1, 2024 |
| Lisdexamfetamine dimesylate | 57664-088 | Tablet, chewable | Generic drugs (ANDA) | August 25, 2023 |
| Lisdexamfetamine dimesylate | 57664-087 | Tablet, chewable | Generic drugs (ANDA) | August 25, 2023 |
| Lisdexamfetamine dimesylate | 57664-086 | Tablet, chewable | Generic drugs (ANDA) | August 25, 2023 |
| Lisdexamfetamine dimesylate | 57664-085 | Tablet, chewable | Generic drugs (ANDA) | August 25, 2023 |
| Lisdexamfetamine dimesylate | 57664-084 | Tablet, chewable | Generic drugs (ANDA) | August 25, 2023 |
| Lisdexamfetamine dimesylate | 57664-083 | Tablet, chewable | Generic drugs (ANDA) | August 25, 2023 |
| Lisdexamfetamine dimesylate | 57664-052 | Capsule | Generic drugs (ANDA) | August 25, 2023 |
| Lisdexamfetamine dimesylate | 57664-051 | Capsule | Generic drugs (ANDA) | August 25, 2023 |
| Lisdexamfetamine dimesylate | 57664-050 | Capsule | Generic drugs (ANDA) | August 25, 2023 |
| Lisdexamfetamine dimesylate | 57664-049 | Capsule | Generic drugs (ANDA) | August 25, 2023 |
| Lisdexamfetamine dimesylate | 57664-048 | Capsule | Generic drugs (ANDA) | August 25, 2023 |
| Lisdexamfetamine dimesylate | 57664-047 | Capsule | Generic drugs (ANDA) | August 25, 2023 |
| Lisdexamfetamine dimesylate | 57664-046 | Capsule | Generic drugs (ANDA) | August 25, 2023 |
| Trazodone Hydrochloride | 57664-053 | Tablet | Generic drugs (ANDA) | October 3, 2022 |
| Trazodone Hydrochloride | 57664-026 | Tablet, film coated | Generic drugs (ANDA) | October 3, 2022 |
| Trazodone Hydrochloride | 57664-014 | Tablet, film coated | Generic drugs (ANDA) | October 3, 2022 |
| Levorphanol Tartrate | 57664-762 | Tablet | Generic drugs (ANDA) | April 26, 2022 |
| Halcinonide | 57664-698 | Cream | Authorized generics (NDA) | May 22, 2021 |
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.