Package 65162-669-50

Brand: acebutolol hydrochloride

Generic: acebutolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 65162-669-50
Digits Only 6516266950
Product NDC 65162-669
Product ID 65162-669_3ff6b39d-7986-49c7-8d95-a2173a28d21c
Description

500 CAPSULE in 1 BOTTLE (65162-669-50)

Marketing

Marketing Status
Marketed Since 2009-12-01
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": "3ff6b39d-7986-49c7-8d95-a2173a28d21c", "openfda": {"upc": ["0365162670103", "0365162669107"], "unii": ["B025Y34C54"], "rxcui": ["998685", "998689"], "spl_set_id": ["28f8c26c-a1e1-4485-a45f-05c82f7a34b5"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (65162-669-10)", "package_ndc": "65162-669-10", "marketing_start_date": "20091201"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (65162-669-50)", "package_ndc": "65162-669-50", "marketing_start_date": "20091201"}], "brand_name": "Acebutolol Hydrochloride", "product_id": "65162-669_3ff6b39d-7986-49c7-8d95-a2173a28d21c", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "65162-669", "generic_name": "Acebutolol Hydrochloride", "labeler_name": "Amneal Pharmaceuticals LLC", "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": "20091201", "listing_expiration_date": "20261231"}