Register entry
Nanoplus Technology Co., Limited
Data as of · How to read this entry
- Registered sites
- 0
- Active NDC listings
- 3
- Live patents
- 0
- Countries
- 0
Catalogue
Drug listings by form and route
33 active NDC listings: 3 human otc drug. By marketing category: UNAPPROVED DRUG OTHER 2, OTC MONOGRAPH DRUG 1.
| Dosage form | NDCs |
|---|---|
| liquid | 3 |
| Route | NDCs |
|---|---|
| topical | 2 |
| ophthalmic | 1 |
| Labeller name on the listing | NDCs |
|---|---|
| nanoplus technology co., limited | 3 |
Catalogue
Marketed products
3| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| OHTrust Artifical Eyedrop | Sodium Chloride | liquid, ophthalmic | 70970-008OTC MONOGRAPH DRUG |
| OHTrust Mouth And Nasal Relief | Hydroxide Ions | liquid, topical | 70970-007UNAPPROVED DRUG OTHER |
| OHTrust Nano Ion Water | Hydroxide Ions | liquid, topical | 70970-006UNAPPROVED DRUG OTHER |
Enquiry
Common questions
- Is Nanoplus Technology Co., Limited FDA approved?
- Nanoplus Technology Co., Limited holds no registered establishment of its own; 3 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
- What drugs does Nanoplus Technology Co., Limited make?
- 3 products are listed under Nanoplus Technology Co., Limited in the openFDA NDC Directory, most often as liquid. 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.