Data / Drug companies / Cumberland Pharmaceuticals Inc.
Cumberland Pharmaceuticals Inc.: 7 products in the FDA NDC directory, labeler code 66220
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Cumberland Pharmaceuticals Inc. (labeler code 66220) lists 7 products in the FDA National Drug Code Directory, covering 5 finished drugs by generic name. By type: 7 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on July 16, 2024.
The request: Watch Cumberland Pharmaceuticals Inc. (FDA labeler code 66220): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 66220
- Products in commercial distribution
- 7
- Packages
- 10
- Finished drugs by generic name
- 5
- Prescription products
- 7
- Over the counter products
- 0
- Flagged as original packager
- 7 of 7 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- January 23, 2004
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| New drug applications (NDA) | 5 | 71.4% |
| Generic drugs (ANDA) | 2 | 28.6% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 7 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Ibuprofen | 2 | 190 |
| Lactulose | 2 | 18 |
| Telavancin hydrochloride | 1 | 1 |
| Acetylcysteine | 1 | 15 |
| Granisetron | 1 | 2 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Injection | 2 | 28.6% |
| Powder, for solution | 2 | 28.6% |
| Injection, powder, lyophilized, for solution | 1 | 14.3% |
| Injection, solution | 1 | 14.3% |
| Patch | 1 | 14.3% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Nonsteroidal Anti-inflammatory Drug | 2 |
| Osmotic Laxative | 2 |
| Lipoglycopeptide Antibacterial | 1 |
| Antidote | 1 |
| Antidote for Acetaminophen Overdose | 1 |
| Mucolytic | 1 |
| Serotonin-3 Receptor Antagonist | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Sancuso | 66220-637 | Patch | New drug applications (NDA) | July 16, 2024 |
| Vibativ | 66220-315 | Injection, powder, lyophilized, for solution | New drug applications (NDA) | January 1, 2021 |
| Caldolor | 66220-284 | Injection | New drug applications (NDA) | January 1, 2020 |
| Kristalose | 66220-729 | Powder, for solution | Generic drugs (ANDA) | January 20, 2012 |
| Kristalose | 66220-719 | Powder, for solution | Generic drugs (ANDA) | January 20, 2012 |
| Caldolor | 66220-287 | Injection | New drug applications (NDA) | June 11, 2009 |
| Acetadote | 66220-207 | Injection, solution | New drug applications (NDA) | January 23, 2004 |
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.