Data / Drug companies / PPL Pharma Solutions Riverview LLC
PPL Pharma Solutions Riverview LLC: 10 products in the FDA NDC directory, labeler code 48957
PPL Pharma Solutions Riverview LLC (labeler code 48957) lists 10 products in the FDA National Drug Code Directory. By type: 10 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on August 14, 2024.
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- Labeler code
- 48957
- Products in commercial distribution
- 10
- Packages
- 10
- Finished drugs by generic name
- 0
- Prescription products
- 0
- Over the counter products
- 0
- Controlled substance products
- Schedule IV 1
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- February 4, 1999
- 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 | 10 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Bulk ingredients | 10 | 100% |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Powder | 10 | 100% |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Seladelpar | 48957-0106 | Powder | Bulk ingredients | August 14, 2024 |
| Zuranolone | 48957-0115 | Powder | Bulk ingredients | October 31, 2023 |
| Mavacamten | 48957-0091 | Powder | Bulk ingredients | April 28, 2022 |
| Cabozantinib (s)-malate | 48957-0121 | Powder | Bulk ingredients | February 26, 2021 |
| Lomitapide mesylate | 48957-0086 | Powder | Bulk ingredients | July 11, 2016 |
| Ixazomib citrate | 48957-0056 | Powder | Bulk ingredients | December 12, 2015 |
| Amotosalen hydrochloride | 48957-0007 | Powder | Bulk ingredients | December 16, 2014 |
| Ponatinib hydrochloride | 48957-0070 | Powder | Bulk ingredients | December 14, 2012 |
| Bortezomib | 48957-0018 | Powder | Bulk ingredients | May 13, 2003 |
| Busulfan | 48957-0010 | Powder | Bulk ingredients | February 4, 1999 |
Updated November 6, 2026. Read from US Food and Drug Administration, National Drug Code Directory (openFDA). 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.