Package 60687-226-01

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60687-226-01
Digits Only 6068722601
Product NDC 60687-226
Description

100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-226-01) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (60687-226-11)

Marketing

Marketing Status
Marketed Since 2017-07-14
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": "3f2c1ac2-1bb2-3613-e063-6394a90a211f", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856535", "856569"], "spl_set_id": ["015b5e4f-3228-4259-b419-e0e49694a058"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-226-01)  / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (60687-226-11)", "package_ndc": "60687-226-01", "marketing_start_date": "20170714"}], "brand_name": "Propranolol Hydrochloride", "product_id": "60687-226_3f2c1ac2-1bb2-3613-e063-6394a90a211f", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "60687-226", "generic_name": "Propranolol Hydrochloride", "labeler_name": "American Health Packaging", "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": "20170714", "listing_expiration_date": "20261231"}