Package 0143-9872-10

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0143-9872-10
Digits Only 0143987210
Product NDC 0143-9872
Description

10 VIAL in 1 CARTON (0143-9872-10) / 1 mL in 1 VIAL (0143-9872-01)

Marketing

Marketing Status
Marketed Since 2008-01-31
Brand propranolol hydrochloride
Generic propranolol hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "4432e36f-bed0-4e42-87aa-1330d1725963", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856443"], "spl_set_id": ["91f2ff1d-68d8-4e83-a2db-618f0410ead7"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (0143-9872-10)  / 1 mL in 1 VIAL (0143-9872-01)", "package_ndc": "0143-9872-10", "marketing_start_date": "20080131"}], "brand_name": "Propranolol Hydrochloride", "product_id": "0143-9872_4432e36f-bed0-4e42-87aa-1330d1725963", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0143-9872", "generic_name": "Propranolol Hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA077760", "marketing_category": "ANDA", "marketing_start_date": "20080131", "listing_expiration_date": "20271231"}