Data / Drug companies / Braintree Laboratories, Inc.
Braintree Laboratories, Inc.: 5 products in the FDA NDC directory, labeler code 52268
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Braintree Laboratories, Inc. (labeler code 52268) lists 5 products in the FDA National Drug Code Directory, covering 2 finished drugs by generic name. By type: 5 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on June 15, 2023.
The request: Watch Braintree Laboratories, Inc. (FDA labeler code 52268): each new product listing and each discontinued product. $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.
- Labeler code
- 52268
- Products in commercial distribution
- 5
- Packages
- 5
- Finished drugs by generic name
- 2
- Prescription products
- 5
- Over the counter products
- 0
- Started marketing in the last 12 months
- 0
- Products with a marketing end date set
- 5
- Earliest marketing start
- July 13, 1984
- 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 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 5 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Sodium sulfate, potassium sulfate, magnesium sulfate | 2 | 6 |
| Sodium sulfate, magnesium sulfate, and potassium chloride | 1 | 2 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Solution, concentrate | 2 | 40% |
| Tablet | 1 | 20% |
| Kit | 1 | 20% |
| Powder, for solution | 1 | 20% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Osmotic Laxative | 4 |
| Potassium Salt | 4 |
| Calculi Dissolution Agent | 3 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Suflave | 52268-550 | Kit | New drug applications (NDA) | June 15, 2023 |
| Sutab | 52268-201 | Tablet | New drug applications (NDA) | November 10, 2020 |
| SUPREP Bowel Prep | 52268-112 | Solution, concentrate | New drug applications (NDA) | August 5, 2010 |
| SUPREP Bowel Prep | 52268-012 | Solution, concentrate | New drug applications (NDA) | August 5, 2010 |
| GoLYTELY | 52268-100 | Powder, for solution | New drug applications (NDA) | July 13, 1984 |
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.