Data / Drug companies / Square Pharmaceuticals Limited
Square Pharmaceuticals Limited: 18 products in the FDA NDC directory, labeler code 76483
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Square Pharmaceuticals Limited (labeler code 76483) lists 18 products in the FDA National Drug Code Directory, covering 8 finished drugs by generic name. By type: 18 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on October 30, 2026.
The request: Watch Square Pharmaceuticals Limited (FDA labeler code 76483): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 76483
- Products in commercial distribution
- 18
- Packages
- 57
- Finished drugs by generic name
- 8
- Prescription products
- 18
- Over the counter products
- 0
- Flagged as original packager
- 17 of 17 products that carry the flag
- Started marketing in the last 12 months
- 2
- Earliest marketing start
- January 31, 2020
- 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 |
|---|---|---|
| Aripiprazole | 4 | 49 |
| Valsartan | 4 | 38 |
| Mirtazapine | 3 | 42 |
| Acyclovir | 2 | 70 |
| Methimazole | 2 | 23 |
| Calcium chloride | 1 | 14 |
| Magnesium sulfate heptahydrate | 1 | 20 |
| Calcium acetate | 1 | 20 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 8 | 44.4% |
| Tablet, orally disintegrating | 7 | 38.9% |
| Injection, solution | 2 | 11.1% |
| Capsule | 1 | 5.6% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Magnesium Sulfate | 76483-129 | Injection, solution | Generic drugs (ANDA) | October 30, 2026 |
| Calcium chloride | 76483-108 | Injection, solution | Generic drugs (ANDA) | January 15, 2026 |
| Methimazole | 76483-083 | Tablet | Generic drugs (ANDA) | December 31, 2024 |
| Methimazole | 76483-082 | Tablet | Generic drugs (ANDA) | December 31, 2024 |
| Calcium Acetate | 76483-086 | Capsule | Generic drugs (ANDA) | May 31, 2023 |
| Mirtazapine | 76483-112 | Tablet, orally disintegrating | Generic drugs (ANDA) | November 15, 2022 |
| Mirtazapine | 76483-111 | Tablet, orally disintegrating | Generic drugs (ANDA) | November 15, 2022 |
| Mirtazapine | 76483-110 | Tablet, orally disintegrating | Generic drugs (ANDA) | November 15, 2022 |
| Aripiprazole | 76483-103 | Tablet, orally disintegrating | Generic drugs (ANDA) | July 20, 2022 |
| Aripiprazole | 76483-102 | Tablet, orally disintegrating | Generic drugs (ANDA) | July 20, 2022 |
| Aripiprazole | 76483-101 | Tablet, orally disintegrating | Generic drugs (ANDA) | July 20, 2022 |
| Aripiprazole | 76483-100 | Tablet, orally disintegrating | Generic drugs (ANDA) | July 20, 2022 |
| Valsartan | 76483-026 | Tablet | Generic drugs (ANDA) | July 15, 2022 |
| Valsartan | 76483-025 | Tablet | Generic drugs (ANDA) | July 15, 2022 |
| Valsartan | 76483-024 | Tablet | Generic drugs (ANDA) | July 15, 2022 |
| Valsartan | 76483-023 | Tablet | Generic drugs (ANDA) | July 15, 2022 |
| Acyclovir | 76483-047 | Tablet | Generic drugs (ANDA) | January 31, 2020 |
| Acyclovir | 76483-042 | Tablet | Generic drugs (ANDA) | January 31, 2020 |
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.