Data / Drug companies / Teva Pharmaceuticals USA, Inc.
Teva Pharmaceuticals USA, Inc.: 12 products in the FDA NDC directory, labeler code 0172
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Teva Pharmaceuticals USA, Inc. (labeler code 0172) lists 12 products in the FDA National Drug Code Directory, covering 6 finished drugs by generic name. By type: 12 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on June 3, 2025.
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- Labeler code
- 0172
- Products in commercial distribution
- 12
- Packages
- 25
- Finished drugs by generic name
- 6
- Prescription products
- 12
- Over the counter products
- 0
- Controlled substance products
- Schedule IV 3
- Flagged as original packager
- 9 of 9 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- January 12, 1973
- 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) | 12 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 12 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Hydrochlorothiazide | 3 | 51 |
| Diazepam | 3 | 51 |
| Baclofen | 2 | 65 |
| Famotidine | 2 | 138 |
| Cromolyn sodium | 1 | 11 |
| Cyclosporine | 1 | 24 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 8 | 66.7% |
| Solution | 2 | 16.7% |
| Tablet, film coated | 2 | 16.7% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Thiazide Diuretic | 3 |
| Benzodiazepine | 3 |
| gamma-Aminobutyric Acid-ergic Agonist | 2 |
| Histamine-2 Receptor Antagonist | 2 |
| Mast Cell Stabilizer | 1 |
| Calcineurin Inhibitor Immunosuppressant | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Hydrochlorothiazide | 0172-3444 | Tablet | Generic drugs (ANDA) | June 3, 2025 |
| Cyclosporine | 0172-7313 | Solution | Generic drugs (ANDA) | March 29, 2005 |
| Famotidine | 0172-5729 | Tablet, film coated | Generic drugs (ANDA) | April 16, 2001 |
| Famotidine | 0172-5728 | Tablet, film coated | Generic drugs (ANDA) | April 16, 2001 |
| Cromolyn Sodium | 0172-6406 | Solution | Generic drugs (ANDA) | January 18, 2000 |
| Baclofen | 0172-4097 | Tablet | Generic drugs (ANDA) | July 21, 1988 |
| Baclofen | 0172-4096 | Tablet | Generic drugs (ANDA) | July 21, 1988 |
| Diazepam | 0172-3927 | Tablet | Generic drugs (ANDA) | December 10, 1986 |
| Diazepam | 0172-3926 | Tablet | Generic drugs (ANDA) | December 10, 1986 |
| Diazepam | 0172-3925 | Tablet | Generic drugs (ANDA) | December 10, 1986 |
| Hydrochlorothiazide | 0172-2089 | Tablet | Generic drugs (ANDA) | January 7, 1980 |
| Hydrochlorothiazide | 0172-2083 | Tablet | Generic drugs (ANDA) | January 12, 1973 |
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.