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EPINASTINE HYDROCHLORIDE
EPINASTINE HYDROCHLORIDE - 62756-329-90 - (EPINASTINE HYDROCHLORIDE)
Drug Information of EPINASTINE HYDROCHLORIDE
| Product NDC: | 62756-329 |
| Proprietary Name: | EPINASTINE HYDROCHLORIDE |
| Non Proprietary Name: | EPINASTINE HYDROCHLORIDE |
| Active Ingredient(s): | .5 mg/mL & nbsp; EPINASTINE HYDROCHLORIDE |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of EPINASTINE HYDROCHLORIDE
| Product NDC: | 62756-329 |
| Labeler Name: | Sun Pharmaceutical Industries Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091626 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111101 |
Package Information of EPINASTINE HYDROCHLORIDE
| Package NDC: | 62756-329-90 |
| Package Description: | 1 BOTTLE in 1 CARTON (62756-329-90) > 5 mL in 1 BOTTLE |
NDC Information of EPINASTINE HYDROCHLORIDE
| NDC Code | 62756-329-90 |
| Proprietary Name | EPINASTINE HYDROCHLORIDE |
| Package Description | 1 BOTTLE in 1 CARTON (62756-329-90) > 5 mL in 1 BOTTLE |
| Product NDC | 62756-329 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | EPINASTINE HYDROCHLORIDE |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20111101 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharmaceutical Industries Limited |
| Substance Name | EPINASTINE HYDROCHLORIDE |
| Strength Number | .5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Adrenergic Agonists [MoA],Adrenergic Receptor Agonist [EPC],Decreased Histamine Release [PE],Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Inhibitor [EPC] |
