NDC 37808-045
Once Daily Relief
Olopatadine Hydrochloride Ophthalmic Solution
Once Daily Relief is a Ophthalmic Solution in the Human Otc Drug category. It is labeled and distributed by H E B. The primary component is Olopatadine Hydrochloride.
Product ID | 37808-045_09597fa5-15e5-0b91-e606-f36426abaed1 |
NDC | 37808-045 |
Product Type | Human Otc Drug |
Proprietary Name | Once Daily Relief |
Generic Name | Olopatadine Hydrochloride Ophthalmic Solution |
Dosage Form | Solution |
Route of Administration | OPHTHALMIC |
Marketing Start Date | 2022-03-07 |
Marketing Category | ANDA / |
Application Number | ANDA209752 |
Labeler Name | H E B |
Substance Name | OLOPATADINE HYDROCHLORIDE |
Active Ingredient Strength | 2 mg/mL |
Pharm Classes | Decreased Histamine Release [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Inhibitor [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2022-12-31 |