Data / Drug companies / Maia Pharmaceuticals, Inc.
Maia Pharmaceuticals, Inc.: 14 products in the FDA NDC directory, labeler code 70511
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Maia Pharmaceuticals, Inc. (labeler code 70511) lists 14 products in the FDA National Drug Code Directory, covering 7 finished drugs by generic name. By type: 14 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on September 8, 2025.
The request: Watch Maia Pharmaceuticals, Inc. (FDA labeler code 70511): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 70511
- Products in commercial distribution
- 14
- Packages
- 15
- Finished drugs by generic name
- 7
- Prescription products
- 14
- Over the counter products
- 0
- Flagged as original packager
- 11 of 11 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- May 22, 2017
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 8 | 57.1% |
| New drug applications (NDA) | 6 | 42.9% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 14 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Baclofen | 4 | 65 |
| Levothyroxine sodium anhydrous | 3 | 6 |
| Sodium phenylacetate and sodium benzoate | 2 | 7 |
| Bortezomib | 2 | 26 |
| Bivalirudin | 1 | 13 |
| Daptomycin | 1 | 25 |
| Sincalide | 1 | 4 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Injection | 7 | 50% |
| Injection, powder, lyophilized, for solution | 5 | 35.7% |
| Injection, solution, concentrate | 1 | 7.1% |
| Injection, solution | 1 | 7.1% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| gamma-Aminobutyric Acid-ergic Agonist | 4 |
| l-Thyroxine | 3 |
| Nitrogen Binding Agent | 2 |
| Proteasome Inhibitor | 2 |
| Anti-coagulant | 1 |
| Direct Thrombin Inhibitor | 1 |
| Lipopeptide Antibacterial | 1 |
| Cholecystokinin Analog | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Daptomycin | 70511-182 | Injection, powder, lyophilized, for solution | New drug applications (NDA) | September 8, 2025 |
| Bivalirudin | 70511-142 | Injection, solution | New drug applications (NDA) | May 27, 2024 |
| Sincalide | 70511-131 | Injection, powder, lyophilized, for solution | New drug applications (NDA) | November 25, 2022 |
| Bortezomib | 70511-161 | Injection | New drug applications (NDA) | August 11, 2022 |
| Bortezomib | 70511-162 | Injection | New drug applications (NDA) | August 10, 2022 |
| Sodium Phenylacetate and Sodium Benzoate | 70511-102 | Injection | New drug applications (NDA) | July 1, 2021 |
| Baclofen | 70511-121 | Injection | Generic drugs (ANDA) | April 2, 2021 |
| Baclofen | 70511-123 | Injection | Generic drugs (ANDA) | December 23, 2020 |
| Baclofen (Intrathecal) | 70511-124 | Injection | Generic drugs (ANDA) | September 25, 2019 |
| Baclofen (Intrathecal) | 70511-122 | Injection | Generic drugs (ANDA) | September 25, 2019 |
| Levothyroxine Sodium | 70511-113 | Injection, powder, lyophilized, for solution | Generic drugs (ANDA) | December 27, 2018 |
| Levothyroxine Sodium | 70511-112 | Injection, powder, lyophilized, for solution | Generic drugs (ANDA) | December 27, 2018 |
| Levothyroxine Sodium | 70511-111 | Injection, powder, lyophilized, for solution | Generic drugs (ANDA) | December 27, 2018 |
| Sodium phenylacetate and sodium benzoate | 70511-101 | Injection, solution, concentrate | Generic drugs (ANDA) | May 22, 2017 |
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.