Package 50090-1501-0

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-1501-0
Digits Only 5009015010
Product NDC 50090-1501
Product ID 50090-1501_b566cbe1-2d29-4d46-bd9c-316e363c9174
Description

30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-1501-0)

Marketing

Marketing Status
Marketed Since 2014-12-08
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": "b566cbe1-2d29-4d46-bd9c-316e363c9174", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856569"], "spl_set_id": ["d1cfdb57-0b04-43f7-bd10-c585f77385b3"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-1501-0)", "package_ndc": "50090-1501-0", "marketing_start_date": "20141208"}], "brand_name": "propranolol hydrochloride", "product_id": "50090-1501_b566cbe1-2d29-4d46-bd9c-316e363c9174", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-1501", "generic_name": "propranolol hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "propranolol hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA078703", "marketing_category": "ANDA", "marketing_start_date": "20130311", "listing_expiration_date": "20261231"}