Register entry
- Registered sites
- 1
- Active NDC listings
- 15
- Live patents
- 0
- Countries
- 1
- Base
- United States
Sites
Registered establishments
1| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| Solaris Pharma Corporation | 49 Napoleon Court, Somerset, New Jersey (NJ) 08873, United States (USA) | Analytical testing | 3012158090079904672 |
Catalogue
Drug listings by form and route
1515 active NDC listings: 15 human prescription drug. By marketing category: ANDA 15.
| Dosage form | NDCs |
|---|---|
| gel | 7 |
| tablet, film coated | 3 |
| tablet | 2 |
| capsule | 1 |
| ointment | 1 |
| tablet, film coated, extended release | 1 |
| Route | NDCs |
|---|---|
| oral | 7 |
| topical | 4 |
| cutaneous | 2 |
| rectal | 1 |
| vaginal | 1 |
| Labeller name on the listing | NDCs |
|---|---|
| solaris pharma corporation | 15 |
Catalogue
Marketed products
15| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| Clarithromycin | Clarithromycin | tablet, film coated, oral | 73473-909ANDA |
| Clarithromycin | Clarithromycin | tablet, film coated, oral | 73473-910ANDA |
| Clarithromycin | Clarithromycin | tablet, film coated, extended release, oral | 73473-911ANDA |
| Clindamycin Phosphate | clindamycin phosphate | gel, topical | 73473-300ANDA |
| Clindamycin Phosphate | clindamycin phosphate | gel, topical | 73473-302ANDA |
| Clindamycin Phosphate and Tretinoin | clindamycin phosphate and tretinoin | gel, topical | 73473-306ANDA |
| DICYCLOMINE HYDROCHLORIDE | DICYCLOMINE HYDROCHLORIDE | capsule, oral | 73473-800ANDA |
| DICYCLOMINE HYDROCHLORIDE | DICYCLOMINE HYDROCHLORIDE | tablet, oral | 73473-902ANDA |
| Estradiol | Estradiol | gel, topical | 73473-308ANDA |
| Metronidazole | Metronidazole | gel, vaginal | 73473-303ANDA |
| Moxifloxacin | moxifloxacin hydrochloride | tablet, film coated, oral | 73473-903ANDA |
| Neomycin Sulfate | Neomycin Sulfate | tablet, oral | 73473-901ANDA |
| Nitroglycerin | Nitroglycerin | ointment, rectal | 73473-500ANDA |
| Tazarotene | Tazarotene | gel, cutaneous | 73473-309ANDA |
| Tazarotene | Tazarotene | gel, cutaneous | 73473-310ANDA |
Neighbours
Registered in the same town
7- SOFIE Co. dba SOFIESomerset, NJ
- L'Oreal USA Products IncSOMERSET, NJ
- Capri Aromatics Pvt LtdSomerset, NJ
- JOM PHARMACEUTICAL SERVICES, LLCSomerset, NJ
- Ameripharma Labs Limited Liability CompanySomerset, NJ
- Invaderm CorporationSomerset, NJ
- Novel Laboratories IncSomerset, NJ
Compare
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- PAI Holdings, LLC1 site · 146 NDC
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- Civica, Inc. dba CivicaRx1 site · 103 NDC
- Leading Pharma, LLC1 site · 82 NDC
Enquiry
Common questions
- Is Solaris Pharma Corporation FDA approved?
- Solaris Pharma Corporation holds 1 FDA-registered establishment in the United States. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.
- Where are Solaris Pharma Corporation's registered sites?
- The FDA register lists Somerset, NJ. Registered operations: analytical testing.
- What drugs does Solaris Pharma Corporation make?
- 15 products are listed under Solaris Pharma Corporation in the openFDA NDC Directory, most often as gel; tablet, film coated; tablet. 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.