Data / Drug companies / Holland Company, Inc.
Holland Company, Inc.: 5 products in the FDA NDC directory, labeler code 51378
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Holland Company, Inc. (labeler code 51378) lists 5 products in the FDA National Drug Code Directory. By type: 5 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on October 3, 1983.
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- Labeler code
- 51378
- Products in commercial distribution
- 5
- Packages
- 6
- Finished drugs by generic name
- 0
- Prescription products
- 0
- Over the counter products
- 0
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- November 27, 1981
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Bulk ingredients | 5 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Bulk ingredients | 5 | 100% |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Powder | 3 | 60% |
| Crystal | 2 | 40% |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Ammonium aluminum sulfate | 51378-801 | Powder | Bulk ingredients | October 3, 1983 |
| Potassium aluminum sulfate | 51378-701 | Powder | Bulk ingredients | October 3, 1983 |
| Potassium aluminum sulfate | 51378-700 | Crystal | Bulk ingredients | October 3, 1983 |
| Aluminum sulfate | 51378-961 | Powder | Bulk ingredients | September 28, 1983 |
| Ammonium aluminum sulfate | 51378-800 | Crystal | Bulk ingredients | November 27, 1981 |
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.