Register entry
- Registered sites
- 0
- Active NDC listings
- 16
- Live patents
- 0
- Countries
- 0
Catalogue
Drug listings by form and route
1616 active NDC listings: 16 human prescription drug. By marketing category: ANDA 15, NDA AUTHORIZED GENERIC 1.
| Dosage form | NDCs |
|---|---|
| tablet, film coated | 8 |
| tablet, sugar coated | 5 |
| tablet, film coated, extended release | 2 |
| tablet, delayed release | 1 |
| Route | NDCs |
|---|---|
| oral | 16 |
| Labeller name on the listing | NDCs |
|---|---|
| zameer pharmaceuticals llc | 16 |
Catalogue
Marketed products
16| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| ChlorproMAZINE Hydrochloride | ChlorproMAZINE Hydrochloride | tablet, sugar coated, oral | 90096-131ANDA |
| ChlorproMAZINE Hydrochloride | ChlorproMAZINE Hydrochloride | tablet, sugar coated, oral | 90096-132ANDA |
| ChlorproMAZINE Hydrochloride | ChlorproMAZINE Hydrochloride | tablet, sugar coated, oral | 90096-133ANDA |
| ChlorproMAZINE Hydrochloride | ChlorproMAZINE Hydrochloride | tablet, sugar coated, oral | 90096-134ANDA |
| ChlorproMAZINE Hydrochloride | ChlorproMAZINE Hydrochloride | tablet, sugar coated, oral | 90096-135ANDA |
| Fluphenazine Hydrochloride | Fluphenazine Hydrochloride | tablet, film coated, oral | 90096-121ANDA |
| Fluphenazine Hydrochloride | Fluphenazine Hydrochloride | tablet, film coated, oral | 90096-122ANDA |
| Fluphenazine Hydrochloride | Fluphenazine Hydrochloride | tablet, film coated, oral | 90096-123ANDA |
| Fluphenazine Hydrochloride | Fluphenazine Hydrochloride | tablet, film coated, oral | 90096-124ANDA |
| Naproxen | Naproxen | tablet, delayed release, oral | 90096-161NDA AUTHORIZED GENERIC |
| Oxcarbazepine | Oxcarbazepine | tablet, film coated, oral | 90096-171ANDA |
| Oxcarbazepine | Oxcarbazepine | tablet, film coated, oral | 90096-172ANDA |
| Oxcarbazepine | Oxcarbazepine | tablet, film coated, oral | 90096-173ANDA |
| Ranolazine | ranolazine | tablet, film coated, extended release, oral | 90096-151ANDA |
| Ranolazine | ranolazine | tablet, film coated, extended release, oral | 90096-152ANDA |
| Trospium Chloride | Trospium Chloride | tablet, film coated, oral | 90096-141ANDA |
Enquiry
Common questions
- Is Zameer Pharmaceuticals LLC FDA approved?
- Zameer Pharmaceuticals LLC holds no registered establishment of its own; 16 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
- What drugs does Zameer Pharmaceuticals LLC make?
- 16 products are listed under Zameer Pharmaceuticals LLC in the openFDA NDC Directory, most often as tablet, film coated; tablet, sugar coated; tablet, film coated, extended release. The full breakdown by dosage form and route is above. A listing count is not a sales figure.
Compiled from FDA establishment registrations, the openFDA NDC Directory, the Orange Book and the FDA drug shortage database. Not claimed by the company. Sources and methodology.