Package 42291-010-01

Brand: acebutolol hydrochloride

Generic: acebutolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42291-010-01
Digits Only 4229101001
Product NDC 42291-010
Product ID 42291-010_48481cfc-a410-bc0a-e063-6294a90a7baf
Description

100 CAPSULE in 1 BOTTLE (42291-010-01)

Marketing

Marketing Status
Marketed Since 2023-04-26
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": "48481cfc-a410-bc0a-e063-6294a90a7baf", "openfda": {"unii": ["B025Y34C54"], "rxcui": ["998689"], "spl_set_id": ["fa40a564-a579-15c1-e053-6294a90ad8e9"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (42291-010-01)", "package_ndc": "42291-010-01", "marketing_start_date": "20230426"}], "brand_name": "Acebutolol Hydrochloride", "product_id": "42291-010_48481cfc-a410-bc0a-e063-6294a90a7baf", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "42291-010", "generic_name": "Acebutolol Hydrochloride", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acebutolol Hydrochloride", "active_ingredients": [{"name": "ACEBUTOLOL HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA075047", "marketing_category": "ANDA", "marketing_start_date": "20230426", "listing_expiration_date": "20271231"}