Data / Drug companies / Zameer Pharmaceuticals LLC
Zameer Pharmaceuticals LLC: 16 products in the FDA NDC directory, labeler code 90096
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Zameer Pharmaceuticals LLC (labeler code 90096) lists 16 products in the FDA National Drug Code Directory, covering 6 finished drugs by generic name. By type: 16 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on July 6, 2026.
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- Labeler code
- 90096
- Products in commercial distribution
- 16
- Packages
- 16
- Finished drugs by generic name
- 6
- Prescription products
- 16
- Over the counter products
- 0
- Flagged as original packager
- 13 of 13 products that carry the flag
- Started marketing in the last 12 months
- 4
- Earliest marketing start
- January 1, 2022
- 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) | 15 | 93.8% |
| Authorized generics (NDA) | 1 | 6.2% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 16 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Chlorpromazine hydrochloride | 5 | 27 |
| Fluphenazine hydrochloride | 4 | 29 |
| Oxcarbazepine | 3 | 46 |
| Ranolazine | 2 | 30 |
| Trospium chloride | 1 | 22 |
| Naproxen | 1 | 58 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 8 | 50% |
| Tablet, sugar coated | 5 | 31.2% |
| Tablet, film coated, extended release | 2 | 12.5% |
| Tablet, delayed release | 1 | 6.2% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Phenothiazine | 9 |
| Anti-epileptic Agent | 3 |
| Anti-anginal | 2 |
| Cholinergic Muscarinic Antagonist | 1 |
| Nonsteroidal Anti-inflammatory Drug | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Oxcarbazepine | 90096-173 | Tablet, film coated | Generic drugs (ANDA) | July 6, 2026 |
| Oxcarbazepine | 90096-172 | Tablet, film coated | Generic drugs (ANDA) | July 6, 2026 |
| Oxcarbazepine | 90096-171 | Tablet, film coated | Generic drugs (ANDA) | July 6, 2026 |
| Ranolazine | 90096-151 | Tablet, film coated, extended release | Generic drugs (ANDA) | April 22, 2026 |
| Ranolazine | 90096-152 | Tablet, film coated, extended release | Generic drugs (ANDA) | October 30, 2025 |
| Naproxen | 90096-161 | Tablet, delayed release | Authorized generics (NDA) | August 31, 2025 |
| Trospium Chloride | 90096-141 | Tablet, film coated | Generic drugs (ANDA) | December 3, 2022 |
| ChlorproMAZINE Hydrochloride | 90096-135 | Tablet, sugar coated | Generic drugs (ANDA) | February 5, 2022 |
| ChlorproMAZINE Hydrochloride | 90096-134 | Tablet, sugar coated | Generic drugs (ANDA) | February 5, 2022 |
| ChlorproMAZINE Hydrochloride | 90096-133 | Tablet, sugar coated | Generic drugs (ANDA) | February 5, 2022 |
| ChlorproMAZINE Hydrochloride | 90096-132 | Tablet, sugar coated | Generic drugs (ANDA) | February 5, 2022 |
| ChlorproMAZINE Hydrochloride | 90096-131 | Tablet, sugar coated | Generic drugs (ANDA) | February 5, 2022 |
| Fluphenazine Hydrochloride | 90096-124 | Tablet, film coated | Generic drugs (ANDA) | January 1, 2022 |
| Fluphenazine Hydrochloride | 90096-123 | Tablet, film coated | Generic drugs (ANDA) | January 1, 2022 |
| Fluphenazine Hydrochloride | 90096-122 | Tablet, film coated | Generic drugs (ANDA) | January 1, 2022 |
| Fluphenazine Hydrochloride | 90096-121 | Tablet, film coated | Generic drugs (ANDA) | January 1, 2022 |
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.