Data / Drug companies / Rusan Pharma Ltd
Rusan Pharma Ltd: 5 products in the FDA NDC directory, labeler code 70312
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Rusan Pharma Ltd (labeler code 70312) lists 5 products in the FDA National Drug Code Directory. By type: 5 bulk ingredients. Its main marketing category is bulk ingredients for compounding. The newest product started marketing on April 8, 2026.
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- Labeler code
- 70312
- Products in commercial distribution
- 5
- Packages
- 25
- Finished drugs by generic name
- 0
- Prescription products
- 0
- Over the counter products
- 0
- Started marketing in the last 12 months
- 2
- Earliest marketing start
- December 16, 2015
- 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 for compounding | 5 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Bulk ingredients | 5 | 100% |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Powder | 5 | 100% |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Nalbuphine hydrochloride | 70312-0891 | Powder | Bulk ingredients for compounding | April 8, 2026 |
| Apomorphine hydrochloride | 70312-0890 | Powder | Bulk ingredients for compounding | March 9, 2026 |
| Naltrexone base | 70312-0888 | Powder | Bulk ingredients for compounding | January 19, 2018 |
| Eflornithine hydrochloride monohydrate | 70312-0889 | Powder | Bulk ingredients for compounding | January 4, 2016 |
| Naltrexone hydrochloride | 70312-0887 | Powder | Bulk ingredients for compounding | December 16, 2015 |
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.