Data / Drug companies / Moderna US, Inc.
Moderna US, Inc.: 5 products in the FDA NDC directory, labeler code 80777
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Moderna US, Inc. (labeler code 80777) lists 5 products in the FDA National Drug Code Directory, covering 3 finished drugs by generic name. By type: 5 vaccines. Its main marketing category is biologics (BLA). The newest product started marketing on August 17, 2026.
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- Labeler code
- 80777
- Products in commercial distribution
- 5
- Packages
- 10
- Finished drugs by generic name
- 3
- Prescription products
- 0
- Over the counter products
- 0
- Started marketing in the last 12 months
- 4
- Earliest marketing start
- May 31, 2024
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Biologics (BLA) | 5 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Vaccines | 5 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Covid-19 vaccine, mrna | 3 | 2 |
| Influenza vaccine, mrna | 1 | 1 |
| Respiratory syncytial virus vaccine | 1 | 2 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Injection, suspension | 4 | 80% |
| Suspension | 1 | 20% |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| MNEXSPIKE | 80777-401 | Injection, suspension | Biologics (BLA) | August 17, 2026 |
| Spikevax | 80777-115 | Injection, suspension | Biologics (BLA) | August 17, 2026 |
| Spikevax | 80777-114 | Injection, suspension | Biologics (BLA) | August 17, 2026 |
| MFLUSIVA | 80777-500 | Injection, suspension | Biologics (BLA) | August 5, 2026 |
| MRESVIA | 80777-345 | Suspension | Biologics (BLA) | May 31, 2024 |
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.