Package 50268-663-15

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50268-663-15
Digits Only 5026866315
Product NDC 50268-663
Description

50 BLISTER PACK in 1 BOX (50268-663-15) / 1 TABLET in 1 BLISTER PACK (50268-663-11)

Marketing

Marketing Status
Marketed Since 2023-08-23
Brand propranolol hydrochloride
Generic propranolol hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47fb48ff-0cf3-5853-e063-6294a90a82a7", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856448", "856457", "856519"], "spl_set_id": ["039b415b-094a-da37-e063-6294a90a52d7"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-663-15)  / 1 TABLET in 1 BLISTER PACK (50268-663-11)", "package_ndc": "50268-663-15", "marketing_start_date": "20230823"}], "brand_name": "Propranolol Hydrochloride", "product_id": "50268-663_47fb48ff-0cf3-5853-e063-6294a90a82a7", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50268-663", "generic_name": "Propranolol Hydrochloride", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA071972", "marketing_category": "ANDA", "marketing_start_date": "20230823", "listing_expiration_date": "20271231"}