Data / Drug companies / First Nation Group, LLC
First Nation Group, LLC: 20 products in the FDA NDC directory, labeler code 81469
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
First Nation Group, LLC (labeler code 81469) lists 20 products in the FDA National Drug Code Directory, covering 8 finished drugs by generic name. By type: 17 prescription drugs, 3 over the counter drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on October 2, 2026.
The request: Watch First Nation Group, LLC (FDA labeler code 81469): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 81469
- Products in commercial distribution
- 20
- Packages
- 35
- Finished drugs by generic name
- 8
- Prescription products
- 17
- Over the counter products
- 3
- Flagged as original packager
- 15 of 15 products that carry the flag
- Started marketing in the last 12 months
- 9
- Earliest marketing start
- January 11, 2023
- 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) | 19 | 95% |
| Over the counter monograph drugs | 1 | 5% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 17 | 85% |
| Over the counter drugs | 3 | 15% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Doxepin hydrochloride | 5 | 45 |
| Bumetanide | 3 | 42 |
| Midodrine hydrochloride | 3 | 34 |
| Cetirizine hydrochloride | 2 | 119 |
| Timolol maleate | 2 | 20 |
| Phenylephrine hydrochloride | 2 | 77 |
| Bimatoprost | 1 | 15 |
| Divalproex sodium | 1 | 48 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 8 | 40% |
| Solution/ drops | 5 | 25% |
| Capsule | 5 | 25% |
| Capsule, coated pellets | 1 | 5% |
| Powder, for solution | 1 | 5% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Cetirizine Hydrochloride | 81469-352 | Tablet | Generic drugs (ANDA) | October 2, 2026 |
| Phenylephrine Hydrochloride | 81469-169 | Solution/ drops | Generic drugs (ANDA) | September 1, 2026 |
| Phenylephrine Hydrochloride | 81469-168 | Solution/ drops | Generic drugs (ANDA) | September 1, 2026 |
| Cetirizine Hydrochloride | 81469-353 | Tablet | Generic drugs (ANDA) | May 29, 2026 |
| Bimatoprost | 81469-291 | Solution/ drops | Generic drugs (ANDA) | May 1, 2026 |
| Bumetanide | 81469-223 | Tablet | Generic drugs (ANDA) | February 19, 2026 |
| Bumetanide | 81469-222 | Tablet | Generic drugs (ANDA) | February 19, 2026 |
| Bumetanide | 81469-221 | Tablet | Generic drugs (ANDA) | February 19, 2026 |
| Divalproex sodium | 81469-492 | Capsule, coated pellets | Generic drugs (ANDA) | November 10, 2025 |
| Midodrine Hydrochloride | 81469-141 | Tablet | Generic drugs (ANDA) | August 13, 2025 |
| Midodrine Hydrochloride | 81469-140 | Tablet | Generic drugs (ANDA) | August 13, 2025 |
| Midodrine Hydrochloride | 81469-139 | Tablet | Generic drugs (ANDA) | August 13, 2025 |
| Timolol maleate | 81469-210 | Solution/ drops | Generic drugs (ANDA) | May 10, 2024 |
| Timolol maleate | 81469-209 | Solution/ drops | Generic drugs (ANDA) | May 10, 2024 |
| Astringent Solution | 81469-999 | Powder, for solution | Over the counter monograph drugs | September 27, 2023 |
| Doxepin Hydrochloride | 81469-419 | Capsule | Generic drugs (ANDA) | January 11, 2023 |
| Doxepin Hydrochloride | 81469-418 | Capsule | Generic drugs (ANDA) | January 11, 2023 |
| Doxepin Hydrochloride | 81469-417 | Capsule | Generic drugs (ANDA) | January 11, 2023 |
| Doxepin Hydrochloride | 81469-416 | Capsule | Generic drugs (ANDA) | January 11, 2023 |
| Doxepin Hydrochloride | 81469-415 | Capsule | Generic drugs (ANDA) | January 11, 2023 |
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.