Package 68071-3576-1

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3576-1
Digits Only 6807135761
Product NDC 68071-3576
Product ID 68071-3576_11873c68-b30b-e883-e063-6294a90a2b3c
Description

120 TABLET in 1 BOTTLE, PLASTIC (68071-3576-1)

Marketing

Marketing Status
Marketed Since 2024-02-16
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": "11873c68-b30b-e883-e063-6294a90a2b3c", "openfda": {"upc": ["0368071357615"], "unii": ["F8A3652H1V"], "rxcui": ["856519"], "spl_set_id": ["11873816-5789-e951-e063-6294a90ad16e"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE, PLASTIC (68071-3576-1)", "package_ndc": "68071-3576-1", "marketing_start_date": "20240216"}], "brand_name": "Propranolol Hydrochloride", "product_id": "68071-3576_11873c68-b30b-e883-e063-6294a90a2b3c", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68071-3576", "generic_name": "Propranolol Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA070177", "marketing_category": "ANDA", "marketing_start_date": "19860513", "listing_expiration_date": "20261231"}