AG-OLOPATADINE 0.2% DIN 02564769
Health Canada record
| Active ingredient(s) | OLOPATADINE HYDROCHLORIDE 0.2 % |
|---|---|
| Dosage form | Solution |
| Route | Ophthalmic |
| Schedule | PRESCRIPTION |
| Class | Human |
| ATC | S01GX09 OLOPATADINE |
| Original market date | |
| Current status date | 16-Jan-2026 |
| Source | Health Canada DPD |
Establishment licence of the holder
Angita Pharma Inc. — licence 101870, currently licensed, last inspection rating C (2025-01-13).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing OLOPATADINE HYDROCHLORIDE
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 02560976 | JAMP OLOPATADINE 0.2% | JAMP PHARMA CORPORATION | Solution | OLOPATADINE HYDROCHLORIDE 0.2 % | Approved |
| 02531186 | RYALTRIS | GLENMARK SPECIALTY SA | Spray (Metered-Dose) | OLOPATADINE HYDROCHLORIDE 665 MCG; MOMETASONE FUROATE (MOMETASONE FUROATE MONOHYDRATE) 25 MCG | Marketed |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|---|---|---|
| 36739 | 2026-01-16 | Abbreviated New Drug Submission (ANDS) | Administrative: Licensing Agreement between two manufacturers |
International API supply for OLOPATADINE HYDROCHLORIDE
10 active FDA Drug Master Files.
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