Data / Drug companies / Ibuprofen and famotidine
Ibuprofen and famotidine: 14 companies and 19 products in the FDA NDC directory
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Ibuprofen and famotidine is listed in the FDA National Drug Code Directory by 14 companies, with 19 products in commercial distribution. 19 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; tablet, and the newest product started marketing on June 18, 2026.
The request: Get every company that lists ibuprofen and famotidine in the FDA NDC directory, with headquarters, website and number of employees. $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.
- Companies listing it
- 14
- Products
- 19
- Generic (ANDA) products
- 19 (100.0%)
- Application numbers
- 5
- Routes
- Oral
- openFDA record search
- api.fda.gov
Companies that list ibuprofen and famotidine
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Advanced Rx of Tennessee, LLC | 4 | tablet; tablet, film coated | Generic drugs (ANDA) | June 18, 2026 |
| Phoenix RX LLC | 3 | tablet, film coated; tablet | Generic drugs (ANDA) | March 15, 2023 |
| Ascend Laboratories, LLC | 1 | tablet, film coated | Generic drugs (ANDA) | August 4, 2021 |
| Ascent Pharmaceuticals, Inc. | 1 | tablet | Generic drugs (ANDA) | October 6, 2022 |
| Asclemed USA, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | August 4, 2021 |
| Aurobindo Pharma Limited | 1 | tablet, film coated | Generic drugs (ANDA) | June 30, 2025 |
| Bryant Ranch Prepack | 1 | tablet, film coated | Generic drugs (ANDA) | August 4, 2021 |
| Camber Pharmaceuticals, Inc. | 1 | tablet | Generic drugs (ANDA) | March 15, 2023 |
| Doc Rx | 1 | tablet, film coated | Generic drugs (ANDA) | August 4, 2021 |
| Par Health USA, LLC | 1 | tablet | Generic drugs (ANDA) | March 22, 2024 |
| Preferred Pharmaceuticals Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | August 1, 2025 |
| Remedyrepack Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | March 5, 2026 |
| Viona Pharmaceuticals Inc | 1 | tablet | Generic drugs (ANDA) | June 1, 2025 |
| Zydus Lifesciences Limited | 1 | tablet | Generic drugs (ANDA) | June 1, 2025 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 10 | 52.6% |
| Tablet | 9 | 47.4% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 19 | 100% |
Pharmacologic classes
| Class | Products |
|---|---|
| Histamine-2 Receptor Antagonist | 19 |
| Nonsteroidal Anti-inflammatory Drug | 19 |
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.