Package 61314-308-02
Brand: azelastine hydrochloride
Generic: azelastine hydrochloridePackage Facts
Identity
Package NDC
61314-308-02
Digits Only
6131430802
Product NDC
61314-308
Description
1 BOTTLE, PLASTIC in 1 CARTON (61314-308-02) / 6 mL in 1 BOTTLE, PLASTIC
Marketing
Marketing Status
Brand
azelastine hydrochloride
Generic
azelastine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAOCULAR"], "spl_id": "8d1b371d-f84a-4054-9a54-7cde00000f81", "openfda": {"unii": ["0L591QR10I"], "rxcui": ["860805"], "spl_set_id": ["6945fb86-27fb-4bab-8908-98772c6269c5"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (61314-308-02) / 6 mL in 1 BOTTLE, PLASTIC", "package_ndc": "61314-308-02", "marketing_start_date": "20130321"}], "brand_name": "Azelastine Hydrochloride", "product_id": "61314-308_8d1b371d-f84a-4054-9a54-7cde00000f81", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "61314-308", "generic_name": "azelastine hydrochloride", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azelastine Hydrochloride", "active_ingredients": [{"name": "AZELASTINE HYDROCHLORIDE", "strength": ".5 mg/mL"}], "application_number": "ANDA202305", "marketing_category": "ANDA", "marketing_start_date": "20130321", "listing_expiration_date": "20261231"}