Data / Drug companies / PharmPak, Inc.
PharmPak, Inc.: 23 products in the FDA NDC directory, labeler code 54348
PharmPak, Inc. (labeler code 54348) lists 23 products in the FDA National Drug Code Directory, covering 17 finished drugs by generic name. By type: 23 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on August 8, 2019.
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- Labeler code
- 54348
- Products in commercial distribution
- 23
- Packages
- 88
- Finished drugs by generic name
- 17
- Prescription products
- 23
- Over the counter products
- 0
- Controlled substance products
- Schedule IV 1
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- November 29, 2013
- 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) | 22 | 95.7% |
| New drug applications (NDA) | 1 | 4.3% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 23 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Ibuprofen | 3 | 190 |
| Ciprofloxacin | 2 | 41 |
| Metronidazole | 2 | 68 |
| Acyclovir | 2 | 70 |
| Estradiol | 2 | 53 |
| Spironolactone | 1 | 45 |
| Ondansetron hydrochloride | 1 | 48 |
| Azithromycin monohydrate | 1 | 7 |
| Ondansetron | 1 | 52 |
| Lorazepam | 1 | 38 |
| Promethazine | 1 | 1 |
| Prednisone | 1 | 49 |
| Sulfamethoxazole, trimethoprim | 1 | 1 |
| Misoprostol | 1 | 15 |
| Medroxyprogesterone | 1 | 1 |
| Prochlorperazine | 1 | 4 |
| Nitrofurantoin monohydrate | 1 | 2 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 14 | 60.9% |
| Tablet, film coated | 8 | 34.8% |
| Capsule | 1 | 4.3% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Ondansetron Hydrochloride | 54348-821 | Tablet, film coated | Generic drugs (ANDA) | August 8, 2019 |
| Medroxyprogesterone | 54348-805 | Tablet | Generic drugs (ANDA) | July 12, 2019 |
| Metronidazole | 54348-745 | Tablet, film coated | Generic drugs (ANDA) | July 12, 2019 |
| Prednisone | 54348-506 | Tablet | Generic drugs (ANDA) | July 12, 2019 |
| Prochlorperazine | 54348-989 | Tablet | Generic drugs (ANDA) | July 11, 2019 |
| Ibuprofen | 54348-835 | Tablet, film coated | Generic drugs (ANDA) | July 11, 2019 |
| Ibuprofen | 54348-830 | Tablet, film coated | Generic drugs (ANDA) | July 11, 2019 |
| Ibuprofen | 54348-825 | Tablet, film coated | Generic drugs (ANDA) | July 11, 2019 |
| Sulfamethox-TMP DS | 54348-625 | Tablet | Generic drugs (ANDA) | July 11, 2019 |
| Promethazine | 54348-117 | Tablet | Generic drugs (ANDA) | July 11, 2019 |
| Lorazepam | 54348-049 | Tablet | Generic drugs (ANDA) | July 11, 2019 |
| Azithromycin | 54348-857 | Tablet, film coated | Generic drugs (ANDA) | July 10, 2019 |
| Nitrofurantoin Mono | 54348-849 | Capsule | New drug applications (NDA) | July 10, 2019 |
| Ondansetron | 54348-819 | Tablet, film coated | Generic drugs (ANDA) | July 10, 2019 |
| Metronidazole | 54348-740 | Tablet, film coated | Generic drugs (ANDA) | July 10, 2019 |
| Ciprofloxacin | 54348-663 | Tablet | Generic drugs (ANDA) | July 10, 2019 |
| Ciprofloxacin | 54348-662 | Tablet | Generic drugs (ANDA) | July 10, 2019 |
| Misoprostol | 54348-148 | Tablet | Generic drugs (ANDA) | July 10, 2019 |
| Estradiol | 54348-702 | Tablet | Generic drugs (ANDA) | July 9, 2019 |
| Estradiol | 54348-701 | Tablet | Generic drugs (ANDA) | July 9, 2019 |
| Acyclovir | 54348-624 | Tablet | Generic drugs (ANDA) | July 9, 2019 |
| Spironolactone | 54348-340 | Tablet | Generic drugs (ANDA) | July 9, 2019 |
| Acyclovir | 54348-627 | Tablet | Generic drugs (ANDA) | November 29, 2013 |
Updated November 6, 2026. Read from US Food and Drug Administration, National Drug Code Directory (openFDA). 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.