Data / Drug companies / Diphenhydramine citrate and ibuprofen
Diphenhydramine citrate and ibuprofen: 7 companies and 7 products in the FDA NDC directory
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Diphenhydramine citrate and ibuprofen is listed in the FDA National Drug Code Directory by 7 companies, with 7 products in commercial distribution. 5 of the products (71.4%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; tablet, coated, and the newest product started marketing on January 24, 2010.
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- Companies listing it
- 7
- Products
- 7
- Generic (ANDA) products
- 5 (71.4%)
- Application numbers
- 2
- Routes
- Oral
- Brand names
- Advil PM, Care One Ibuprofen PM, Up and Up Ibuprofen PM, Ibuprofen PM, DG Health Ibuprofen PM, Topcare Ibuprofen PM
- openFDA record search
- api.fda.gov
Companies that list diphenhydramine citrate and ibuprofen
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| American Sales Company | 1 | tablet, film coated | Generic drugs (ANDA) | February 20, 2009 |
| CVS Pharmacy | 1 | tablet, film coated | Generic drugs (ANDA) | February 17, 2009 |
| Dolgencorp, Inc. (dollar General & Rexall) | 1 | tablet, film coated | Generic drugs (ANDA) | January 24, 2010 |
| Haleon US Holdings LLC | 1 | tablet, coated | New drug applications (NDA) | December 21, 2005 |
| Select Consumer Group | 1 | tablet, coated | New drug applications (NDA) | December 21, 2005 |
| Target Corporation | 1 | tablet, film coated | Generic drugs (ANDA) | July 10, 2009 |
| Topco Associates LLC | 1 | tablet, film coated | Generic drugs (ANDA) | February 18, 2009 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 5 | 71.4% |
| Tablet, coated | 2 | 28.6% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 5 | 71.4% |
| New drug applications (NDA) | 2 | 28.6% |
Pharmacologic classes
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.