Package 62559-256-01
Brand: acebutolol hydrochloride
Generic: acebutolol hydrochloridePackage Facts
Identity
Package NDC
62559-256-01
Digits Only
6255925601
Product NDC
62559-256
Description
100 CAPSULE in 1 BOTTLE (62559-256-01)
Marketing
Marketing Status
Brand
acebutolol hydrochloride
Generic
acebutolol hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "512c2032-4b9a-4b8c-b360-02f89d62714c", "openfda": {"upc": ["0362559255011", "0362559256018"], "unii": ["B025Y34C54"], "rxcui": ["998685", "998689"], "spl_set_id": ["48bded12-09c7-47f2-b162-ec970a77f2d8"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (62559-256-01)", "package_ndc": "62559-256-01", "marketing_start_date": "20220725"}], "brand_name": "Acebutolol Hydrochloride", "product_id": "62559-256_512c2032-4b9a-4b8c-b360-02f89d62714c", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "62559-256", "generic_name": "Acebutolol Hydrochloride", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acebutolol Hydrochloride", "active_ingredients": [{"name": "ACEBUTOLOL HYDROCHLORIDE", "strength": "400 mg/1"}], "application_number": "ANDA074007", "marketing_category": "ANDA", "marketing_start_date": "20220725", "listing_expiration_date": "20261231"}