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NDC 00280-0065-05 Astepro Allergy 205.5 ug/1 Details
Astepro Allergy 205.5 ug/1
Astepro Allergy is a NASAL SPRAY, METERED in the HUMAN OTC DRUG category. It is labeled and distributed by Bayer HealthCare LLC.. The primary component is AZELASTINE HYDROCHLORIDE.
MedlinePlus Drug Summary
Prescription and nonprescription (over the counter) azelastine nasal spray is used to relieve symptoms of rhinitis such as sneezing and a runny, stuffy, or itchy nose and itchy, watery eyes caused by hay fever or other allergies (caused by an allergy to pollen, mold, dust, or pets). Prescription azelastine nasal spray is also used to relieve symptoms of nonallergic rhinitis such as sneezing and runny or stuffy nose which are not caused by allergies in adults and children 12 years of age or older. Azelastine is in a class of medications called antihistamines. It works by blocking the action of histamine, a substance in the body that causes allergic symptoms.
Related Packages: 00280-0065-05Last Updated: 03/24/2024
MedLinePlus Full Drug Details: Azelastine Nasal Spray
Product Information
| NDC | 00280-0065 |
|---|---|
| Product ID | 0280-0065_05e0474c-67eb-4d5a-e063-6394a90a22fc |
| Associated GPIs | |
| GCN Sequence Number | 065577 |
| GCN Sequence Number Description | azelastine HCl SPRAY/PUMP 205.5 MCG NASAL |
| HIC3 | Q7E |
| HIC3 Description | NASAL ANTIHISTAMINE |
| GCN | 27584 |
| HICL Sequence Number | 007607 |
| HICL Sequence Number Description | AZELASTINE HCL |
| Brand/Generic | Brand |
| Proprietary Name | Astepro Allergy |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Azelastine HCl |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | SPRAY, METERED |
| Route | NASAL |
| Active Ingredient Strength | 205.5 |
| Active Ingredient Units | ug/1 |
| Substance Name | AZELASTINE HYDROCHLORIDE |
| Labeler Name | Bayer HealthCare LLC. |
| Pharmaceutical Class | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
| DEA Schedule | n/a |
| Marketing Category | NDA |
| Application Number | NDA213872 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 00280-0065-05 (00280006505)
| NDC Package Code | 0280-0065-05 |
|---|---|
| Billing NDC | 00280006505 |
| Package | 22 CARTON in 1 BOTTLE (0280-0065-05) / 1 SPRAY, METERED in 1 CARTON |
| Marketing Start Date | 2023-01-24 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |