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Azelastine Hydrochloride
Azelastine Hydrochloride - 60505-0833-5 - (azelastine hydrochloride)
Drug Information of Azelastine Hydrochloride
| Product NDC: | 60505-0833 |
| Proprietary Name: | Azelastine Hydrochloride |
| Non Proprietary Name: | azelastine hydrochloride |
| Active Ingredient(s): | 137 ug/1 & nbsp; azelastine hydrochloride |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY, METERED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Azelastine Hydrochloride
| Product NDC: | 60505-0833 |
| Labeler Name: | Apotex Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077954 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100301 |
Package Information of Azelastine Hydrochloride
| Package NDC: | 60505-0833-5 |
| Package Description: | 1 BOTTLE, SPRAY in 1 CARTON (60505-0833-5) > 200 SPRAY, METERED in 1 BOTTLE, SPRAY |
NDC Information of Azelastine Hydrochloride
| NDC Code | 60505-0833-5 |
| Proprietary Name | Azelastine Hydrochloride |
| Package Description | 1 BOTTLE, SPRAY in 1 CARTON (60505-0833-5) > 200 SPRAY, METERED in 1 BOTTLE, SPRAY |
| Product NDC | 60505-0833 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | azelastine hydrochloride |
| Dosage Form Name | SPRAY, METERED |
| Route Name | NASAL |
| Start Marketing Date | 20100301 |
| Marketing Category Name | ANDA |
| Labeler Name | Apotex Corp. |
| Substance Name | AZELASTINE HYDROCHLORIDE |
| Strength Number | 137 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Inhibitor [EPC] |
