Data / Drug companies / Granules USA, Inc.
Granules USA, Inc.: 14 products in the FDA NDC directory, labeler code 69848
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Granules USA, Inc. (labeler code 69848) lists 14 products in the FDA National Drug Code Directory, covering 10 finished drugs by generic name. By type: 14 over the counter drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on December 10, 2024.
The request: Watch Granules USA, Inc. (FDA labeler code 69848): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 69848
- Products in commercial distribution
- 14
- Packages
- 23
- Finished drugs by generic name
- 10
- Prescription products
- 0
- Over the counter products
- 14
- Flagged as original packager
- 14 of 14 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- July 1, 2018
- 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) | 9 | 64.3% |
| Over the counter monograph drugs | 5 | 35.7% |
Products by type
| Type | Products | Share |
|---|---|---|
| Over the counter drugs | 14 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Acetaminophen | 3 | 214 |
| Guaifenesin | 2 | 123 |
| Ibuprofen | 2 | 190 |
| Acetaminophen diphenhydramine hcl | 1 | 7 |
| Sennosides | 1 | 65 |
| Loratadine | 1 | 125 |
| Clotrimazole | 1 | 98 |
| Acetaminophen and ibuprofen | 1 | 19 |
| Naproxen sodium | 1 | 100 |
| Cetirizine hydrochloride | 1 | 119 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 9 | 64.3% |
| Tablet, extended release | 2 | 14.3% |
| Capsule, liquid filled | 1 | 7.1% |
| Tablet, film coated, extended release | 1 | 7.1% |
| Solution | 1 | 7.1% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Nonsteroidal Anti-inflammatory Drug | 4 |
| Histamine-1 Receptor Antagonist | 2 |
| Expectorant | 2 |
| Azole Antifungal | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Aacetaminophen and Ibuprofen | 69848-588 | Tablet | Generic drugs (ANDA) | December 10, 2024 |
| Guaifenesin | 69848-018 | Tablet, extended release | Generic drugs (ANDA) | September 12, 2024 |
| Guaifenesin | 69848-017 | Tablet, extended release | Generic drugs (ANDA) | December 31, 2021 |
| Loratadine | 69848-019 | Tablet | Generic drugs (ANDA) | July 26, 2021 |
| Cetirizine Hydrochloride | 69848-006 | Tablet | Generic drugs (ANDA) | June 30, 2021 |
| Sennosides | 69848-016 | Capsule, liquid filled | Over the counter monograph drugs | May 29, 2020 |
| Acetaminophen | 69848-008 | Tablet | Over the counter monograph drugs | May 1, 2020 |
| Acetaminophen | 69848-015 | Tablet, film coated, extended release | Generic drugs (ANDA) | December 31, 2019 |
| Acetaminophen Diphenhydramine HCl | 69848-014 | Tablet | Over the counter monograph drugs | July 1, 2019 |
| Ibuprofen | 69848-012 | Tablet | Generic drugs (ANDA) | July 1, 2019 |
| Ibuprofen | 69848-011 | Tablet | Generic drugs (ANDA) | July 1, 2019 |
| Naproxen Sodium | 69848-010 | Tablet | Generic drugs (ANDA) | July 1, 2019 |
| Acetaminophen | 69848-003 | Tablet | Over the counter monograph drugs | July 1, 2019 |
| Clotrimazole | 69848-001 | Solution | Over the counter monograph drugs | July 1, 2018 |
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.