Package 68788-7860-3

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68788-7860-3
Digits Only 6878878603
Product NDC 68788-7860
Description

30 TABLET in 1 BOTTLE (68788-7860-3)

Marketing

Marketing Status
Marketed Since 2021-02-08
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": "e950e99d-b2b0-4d20-ad5f-a20f055463e9", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856448"], "spl_set_id": ["86c48c5a-0a59-43a7-b3b5-41ab5da72ce1"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-7860-3)", "package_ndc": "68788-7860-3", "marketing_start_date": "20210208"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-7860-9)", "package_ndc": "68788-7860-9", "marketing_start_date": "20240802"}], "brand_name": "Propranolol Hydrochloride", "product_id": "68788-7860_e950e99d-b2b0-4d20-ad5f-a20f055463e9", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68788-7860", "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": "10 mg/1"}], "application_number": "ANDA070322", "marketing_category": "ANDA", "marketing_start_date": "20210208", "listing_expiration_date": "20261231"}