Package 47335-938-90
Brand: azelastine hydrochloride
Generic: azelastine hydrochloridePackage Facts
Identity
Package NDC
47335-938-90
Digits Only
4733593890
Product NDC
47335-938
Description
1 BOTTLE, PLASTIC in 1 BOX (47335-938-90) / 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": "b2bdb49f-ef3d-467d-aa3b-d7ab72162f4b", "openfda": {"upc": ["0347335938906"], "unii": ["0L591QR10I"], "rxcui": ["860805"], "spl_set_id": ["04e5eede-17ff-4765-af77-d46c139da703"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (47335-938-90) / 6 mL in 1 BOTTLE, PLASTIC", "package_ndc": "47335-938-90", "marketing_start_date": "20100531"}], "brand_name": "Azelastine Hydrochloride", "product_id": "47335-938_b2bdb49f-ef3d-467d-aa3b-d7ab72162f4b", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "47335-938", "generic_name": "Azelastine Hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azelastine Hydrochloride", "active_ingredients": [{"name": "AZELASTINE HYDROCHLORIDE", "strength": ".5 mg/mL"}], "application_number": "ANDA078738", "marketing_category": "ANDA", "marketing_start_date": "20100531", "listing_expiration_date": "20261231"}