Data / Drug companies / Ani Pharmaceuticals, Inc.
Ani Pharmaceuticals, Inc.: 17 products in the FDA NDC directory, labeler code 43975
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Ani Pharmaceuticals, Inc. (labeler code 43975) lists 17 products in the FDA National Drug Code Directory, covering 5 finished drugs by generic name. By type: 17 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on March 16, 2020.
The request: Watch Ani Pharmaceuticals, Inc. (FDA labeler code 43975): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 43975
- Products in commercial distribution
- 17
- Packages
- 23
- Finished drugs by generic name
- 5
- Prescription products
- 17
- Over the counter products
- 0
- Controlled substance products
- Schedule II 6
- Flagged as original packager
- 17 of 17 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- April 17, 2018
- 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) | 17 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 17 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Paliperidone | 4 | 19 |
| Fenofibrate | 3 | 56 |
| Tolterodine tartrate | 2 | 13 |
| Bexarotene | 1 | 8 |
| Miglustat | 1 | 7 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Capsule, extended release | 8 | 47.1% |
| Capsule | 4 | 23.5% |
| Tablet, extended release | 4 | 23.5% |
| Capsule, liquid filled | 1 | 5.9% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate | 43975-282 | Capsule, extended release | Generic drugs (ANDA) | March 16, 2020 |
| Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate | 43975-281 | Capsule, extended release | Generic drugs (ANDA) | March 16, 2020 |
| Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate | 43975-280 | Capsule, extended release | Generic drugs (ANDA) | March 16, 2020 |
| Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate | 43975-279 | Capsule, extended release | Generic drugs (ANDA) | March 16, 2020 |
| Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate | 43975-278 | Capsule, extended release | Generic drugs (ANDA) | March 16, 2020 |
| Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate | 43975-277 | Capsule, extended release | Generic drugs (ANDA) | March 16, 2020 |
| Paliperidone | 43975-352 | Tablet, extended release | Generic drugs (ANDA) | November 27, 2019 |
| Paliperidone | 43975-351 | Tablet, extended release | Generic drugs (ANDA) | November 27, 2019 |
| Paliperidone | 43975-350 | Tablet, extended release | Generic drugs (ANDA) | November 27, 2019 |
| Paliperidone | 43975-349 | Tablet, extended release | Generic drugs (ANDA) | November 27, 2019 |
| Tolterodine Tartrate | 43975-323 | Capsule, extended release | Generic drugs (ANDA) | August 29, 2019 |
| Tolterodine Tartrate | 43975-322 | Capsule, extended release | Generic drugs (ANDA) | August 29, 2019 |
| Bexarotene | 43975-315 | Capsule, liquid filled | Generic drugs (ANDA) | May 10, 2018 |
| Fenofibrate | 43975-444 | Capsule | Generic drugs (ANDA) | May 1, 2018 |
| Fenofibrate | 43975-306 | Capsule | Generic drugs (ANDA) | May 1, 2018 |
| Fenofibrate | 43975-305 | Capsule | Generic drugs (ANDA) | May 1, 2018 |
| Miglustat | 43975-310 | Capsule | Generic drugs (ANDA) | April 17, 2018 |
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.