Package 0527-4119-41

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0527-4119-41
Digits Only 0527411941
Product NDC 0527-4119
Product ID 0527-4119_ceeffec9-095b-4081-b268-7869b0685921
Description

500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0527-4119-41)

Marketing

Marketing Status
Marketed Since 2020-01-06
Brand propranolol hydrochloride
Generic propranolol hydrochloride
Sample Package No

Linked Drug Pages (1)

Propranolol Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ceeffec9-095b-4081-b268-7869b0685921", "openfda": {"upc": ["0305274116373"], "unii": ["F8A3652H1V"], "rxcui": ["856460", "856481", "856535", "856569"], "spl_set_id": ["5229b561-287b-463c-8679-cda4c34f440b"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0527-4119-37)", "package_ndc": "0527-4119-37", "marketing_start_date": "20200106"}, {"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0527-4119-41)", "package_ndc": "0527-4119-41", "marketing_start_date": "20200106"}], "brand_name": "Propranolol Hydrochloride", "product_id": "0527-4119_ceeffec9-095b-4081-b268-7869b0685921", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0527-4119", "generic_name": "propranolol hydrochloride", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "160 mg/1"}], "application_number": "ANDA212026", "marketing_category": "ANDA", "marketing_start_date": "20200106", "listing_expiration_date": "20261231"}