Data / Drug companies / Larkspur Enterprises LLC
Larkspur Enterprises LLC: 8 products in the FDA NDC directory, labeler code 87126
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Larkspur Enterprises LLC (labeler code 87126) lists 8 products in the FDA National Drug Code Directory. By type: 8 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on January 1, 2026.
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- Labeler code
- 87126
- Products in commercial distribution
- 8
- Packages
- 22
- Finished drugs by generic name
- 0
- Prescription products
- 0
- Over the counter products
- 0
- Started marketing in the last 12 months
- 5
- Products with a marketing end date set
- 8
- Earliest marketing start
- October 1, 2025
- 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 | 8 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Bulk ingredients | 8 | 100% |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Powder | 5 | 62.5% |
| Powder, for solution | 3 | 37.5% |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Gelucire 44/14 | 87126-023 | Powder, for solution | Bulk ingredients | January 1, 2026 |
| Poloxamer 407 | 87126-019 | Powder | Bulk ingredients | January 1, 2026 |
| Pvp k30 | 87126-018 | Powder | Bulk ingredients | December 1, 2025 |
| Peg 6000 | 87126-017 | Powder | Bulk ingredients | December 1, 2025 |
| Syloid 244 fp | 87126-016 | Powder | Bulk ingredients | December 1, 2025 |
| Lidocaine | 87126-301 | Powder | Bulk ingredients | October 1, 2025 |
| Nanosil | 87126-015 | Powder, for solution | Bulk ingredients | October 1, 2025 |
| Ts-88 | 87126-014 | Powder, for solution | Bulk ingredients | October 1, 2025 |
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.