Package 68788-7791-3

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68788-7791-3
Digits Only 6878877913
Product NDC 68788-7791
Product ID 68788-7791_8d251c03-02c2-4dff-942c-8133bcb99925
Description

30 TABLET in 1 BOTTLE (68788-7791-3)

Marketing

Marketing Status
Marketed Since 2020-10-21
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": "8d251c03-02c2-4dff-942c-8133bcb99925", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856457"], "spl_set_id": ["582fe781-0759-4622-8fa6-b7d90e94e696"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-7791-3)", "package_ndc": "68788-7791-3", "marketing_start_date": "20201021"}], "brand_name": "Propranolol Hydrochloride", "product_id": "68788-7791_8d251c03-02c2-4dff-942c-8133bcb99925", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68788-7791", "generic_name": "Propranolol Hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA070322", "marketing_category": "ANDA", "marketing_start_date": "20201021", "listing_expiration_date": "20261231"}