Package 62559-255-01

Brand: acebutolol hydrochloride

Generic: acebutolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62559-255-01
Digits Only 6255925501
Product NDC 62559-255
Product ID 62559-255_512c2032-4b9a-4b8c-b360-02f89d62714c
Description

100 CAPSULE in 1 BOTTLE (62559-255-01)

Marketing

Marketing Status
Marketed Since 2022-07-25
Brand acebutolol hydrochloride
Generic acebutolol hydrochloride
Sample Package No

Linked Drug Pages (1)

Acebutolol Hydrochloride ndc-match (0.95)

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 (62559-255-01)", "package_ndc": "62559-255-01", "marketing_start_date": "20220725"}], "brand_name": "Acebutolol Hydrochloride", "product_id": "62559-255_512c2032-4b9a-4b8c-b360-02f89d62714c", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "62559-255", "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": "200 mg/1"}], "application_number": "ANDA074007", "marketing_category": "ANDA", "marketing_start_date": "20220725", "listing_expiration_date": "20261231"}