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Optivar
Optivar - 0037-7025-60 - (Azelastine Hydrochloride)
Drug Information of Optivar
| Product NDC: | 0037-7025 |
| Proprietary Name: | Optivar |
| Non Proprietary Name: | Azelastine Hydrochloride |
| Active Ingredient(s): | .5 mg/mL & nbsp; Azelastine Hydrochloride |
| Administration Route(s): | INTRAOCULAR |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Optivar
| Product NDC: | 0037-7025 |
| Labeler Name: | Meda Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021127 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20000522 |
Package Information of Optivar
| Package NDC: | 0037-7025-60 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 BOX (0037-7025-60) > 6 mL in 1 BOTTLE, PLASTIC |
NDC Information of Optivar
| NDC Code | 0037-7025-60 |
| Proprietary Name | Optivar |
| Package Description | 1 BOTTLE, PLASTIC in 1 BOX (0037-7025-60) > 6 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 0037-7025 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Azelastine Hydrochloride |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | INTRAOCULAR |
| Start Marketing Date | 20000522 |
| Marketing Category Name | NDA |
| Labeler Name | Meda Pharmaceuticals Inc. |
| Substance Name | AZELASTINE HYDROCHLORIDE |
| Strength Number | .5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Inhibitor [EPC] |
