Medicine passport
Naltrexone Hydrochloride 50 mg
The same active substance, strength and form as listed by each country’s medicines regulator. For showing a pharmacist abroad.
- Active substance
- Naltrexone Hydrochloride
- Strength
- 50 mg
- Form
- Tablet, Film Coated
- ATC code
- Not stated by the register
- Registered in
- United States · Sun Pharmaceutical Industries, Inc.
- Prescription
- Prescription only
- NDC
- 47335-326
Source: NDC Directory · 2026-09-13
Not a prescription. Not a statement that these products are interchangeable. Products are matched on active substance, strength and kind of form only. Other ingredients, release, approved uses and the dose on the box can differ. A pharmacist or doctor decides whether one can replace another.
Listed in other countries
Canada 4 matching products
| Name on the box | Strength and form | Prescription | Holder | Official record |
|---|---|---|---|---|
| APO-NALTREXONE | 50 mg · tablet | Prescription only | Apotex Inc | 02444275 |
| NALTREXONE HYDROCHLORIDE TABLETS USP | 50 mg · tablet | Prescription only | Sterinova Inc. | 02451883 |
| REVIA | 50 mg · tablet | Prescription only | Teva Canada Limited | 02213826 |
| RPC-NALTREXONE | 50 mg · tablet | Prescription only | Rusan Pharma Canada Inc. | 02558343 |
Source: Drug Product Database (Health Canada) · 2026-09-30 · Contains information licensed under the Open Government Licence – Canada.