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PATADAY
PATADAY - 0065-0272-25 - (olopatadine hydrochloride)
Drug Information of PATADAY
| Product NDC: | 0065-0272 |
| Proprietary Name: | PATADAY |
| Non Proprietary Name: | olopatadine hydrochloride |
| Active Ingredient(s): | 2 mg/mL & nbsp; olopatadine hydrochloride |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PATADAY
| Product NDC: | 0065-0272 |
| Labeler Name: | Alcon Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021545 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20070215 |
Package Information of PATADAY
| Package NDC: | 0065-0272-25 |
| Package Description: | 2.5 mL in 1 BOTTLE, PLASTIC (0065-0272-25) |
NDC Information of PATADAY
| NDC Code | 0065-0272-25 |
| Proprietary Name | PATADAY |
| Package Description | 2.5 mL in 1 BOTTLE, PLASTIC (0065-0272-25) |
| Product NDC | 0065-0272 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | olopatadine hydrochloride |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20070215 |
| Marketing Category Name | NDA |
| Labeler Name | Alcon Laboratories, Inc. |
| Substance Name | OLOPATADINE HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Decreased Histamine Release [PE],Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Inhibitor [EPC] |
