Package 50268-050-15

Brand: acebutolol hydrochloride

Generic: acebutolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50268-050-15
Digits Only 5026805015
Product NDC 50268-050
Product ID 50268-050_3f158c97-90b4-1c5e-e063-6294a90a6a65
Description

50 BLISTER PACK in 1 BOX (50268-050-15) / 1 CAPSULE in 1 BLISTER PACK (50268-050-11)

Marketing

Marketing Status
Marketed Since 2010-09-16
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": "3f158c97-90b4-1c5e-e063-6294a90a6a65", "openfda": {"unii": ["B025Y34C54"], "rxcui": ["998689"], "spl_set_id": ["ff68a002-d46d-4f9f-0705-427844ea3655"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-050-15)  / 1 CAPSULE in 1 BLISTER PACK (50268-050-11)", "package_ndc": "50268-050-15", "marketing_start_date": "20100916"}], "brand_name": "Acebutolol Hydrochloride", "product_id": "50268-050_3f158c97-90b4-1c5e-e063-6294a90a6a65", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50268-050", "generic_name": "Acebutolol Hydrochloride", "labeler_name": "AvPAK", "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": "20100916", "listing_expiration_date": "20261231"}