Data / Drug companies / Archis Pharma LLC
Archis Pharma LLC: 18 products in the FDA NDC directory, labeler code 72819
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Archis Pharma LLC (labeler code 72819) lists 18 products in the FDA National Drug Code Directory, covering 9 finished drugs by generic name. By type: 18 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on January 25, 2025.
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- Labeler code
- 72819
- Products in commercial distribution
- 18
- Packages
- 22
- Finished drugs by generic name
- 9
- Prescription products
- 18
- Over the counter products
- 0
- Flagged as original packager
- 18 of 18 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- August 1, 2021
- 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) | 18 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 18 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Mitomycin | 4 | 14 |
| Paliperidone | 3 | 19 |
| Mycophenilic acid | 2 | 1 |
| Doxepin | 2 | 8 |
| Imatinib mesylate | 2 | 17 |
| Cupric chloride | 2 | 7 |
| Nicardipine hydrochloride | 1 | 27 |
| Diclofenac potassium | 1 | 42 |
| Chromic chloride | 1 | 2 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Injection, solution | 4 | 22.2% |
| Injection, powder, lyophilized, for solution | 4 | 22.2% |
| Tablet, film coated | 3 | 16.7% |
| Tablet, film coated, extended release | 3 | 16.7% |
| Tablet, delayed release | 2 | 11.1% |
| Tablet | 2 | 11.1% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Chromic chloride | 72819-235 | Injection, solution | Generic drugs (ANDA) | January 25, 2025 |
| Nicardipine Hydrochloride | 72819-149 | Injection, solution | Generic drugs (ANDA) | December 7, 2024 |
| Cupric chloride | 72819-234 | Injection, solution | Generic drugs (ANDA) | October 1, 2024 |
| Cupric chloride | 72819-234 | Injection, solution | Generic drugs (ANDA) | July 5, 2024 |
| Imatinib mesylate | 72819-186 | Tablet | Generic drugs (ANDA) | September 1, 2022 |
| Imatinib mesylate | 72819-185 | Tablet | Generic drugs (ANDA) | September 1, 2022 |
| Paliperidone | 72819-160 | Tablet, film coated, extended release | Generic drugs (ANDA) | April 27, 2022 |
| Paliperidone | 72819-159 | Tablet, film coated, extended release | Generic drugs (ANDA) | April 27, 2022 |
| Paliperidone | 72819-158 | Tablet, film coated, extended release | Generic drugs (ANDA) | April 27, 2022 |
| Mitomycin | 72819-154 | Injection, powder, lyophilized, for solution | Generic drugs (ANDA) | April 25, 2022 |
| Mitomycin | 72819-153 | Injection, powder, lyophilized, for solution | Generic drugs (ANDA) | April 25, 2022 |
| Mitomycin | 72819-152 | Injection, powder, lyophilized, for solution | Generic drugs (ANDA) | April 25, 2022 |
| Mitomycin | 72819-152 | Injection, powder, lyophilized, for solution | Generic drugs (ANDA) | March 11, 2022 |
| Doxepin | 72819-161 | Tablet, film coated | Generic drugs (ANDA) | February 21, 2022 |
| Mycophenolic Acid | 72819-156 | Tablet, delayed release | Generic drugs (ANDA) | February 21, 2022 |
| Mycophenolic Acid | 72819-155 | Tablet, delayed release | Generic drugs (ANDA) | February 21, 2022 |
| Diclofenac Potassium | 72819-151 | Tablet, film coated | Generic drugs (ANDA) | September 15, 2021 |
| Doxepin | 72819-162 | Tablet, film coated | Generic drugs (ANDA) | August 1, 2021 |
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.