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Olopatadine Hydrochloride
Olopatadine Hydrochloride - 61314-320-01 - (olopatadine hydrochloride)
Drug Information of Olopatadine Hydrochloride
| Product NDC: | 61314-320 |
| Proprietary Name: | Olopatadine Hydrochloride |
| Non Proprietary Name: | olopatadine hydrochloride |
| Active Ingredient(s): | 665 ug/100uL & nbsp; olopatadine hydrochloride |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY, METERED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Olopatadine Hydrochloride
| Product NDC: | 61314-320 |
| Labeler Name: | Falcon Pharmaceuticals, Ltd. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021861 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20120630 |
Package Information of Olopatadine Hydrochloride
| Package NDC: | 61314-320-01 |
| Package Description: | 30500 uL in 1 BOTTLE (61314-320-01) |
NDC Information of Olopatadine Hydrochloride
| NDC Code | 61314-320-01 |
| Proprietary Name | Olopatadine Hydrochloride |
| Package Description | 30500 uL in 1 BOTTLE (61314-320-01) |
| Product NDC | 61314-320 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | olopatadine hydrochloride |
| Dosage Form Name | SPRAY, METERED |
| Route Name | NASAL |
| Start Marketing Date | 20120630 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Falcon Pharmaceuticals, Ltd. |
| Substance Name | OLOPATADINE HYDROCHLORIDE |
| Strength Number | 665 |
| Strength Unit | ug/100uL |
| Pharmaceutical Classes | Decreased Histamine Release [PE],Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Inhibitor [EPC] |
