Package 76420-384-20
Brand: propranolol hydrochloride
Generic: propranolol hydrochloridePackage Facts
Identity
Package NDC
76420-384-20
Digits Only
7642038420
Product NDC
76420-384
Description
20 TABLET in 1 BOTTLE (76420-384-20)
Marketing
Marketing Status
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": "366b6b94-8ad2-8ec9-e063-6394a90a813b", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856448", "856457", "856519", "856556", "856578"], "spl_set_id": ["d08dbabc-8ca4-426e-a9fd-e7914a27883c"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (76420-384-00)", "package_ndc": "76420-384-00", "marketing_start_date": "20250331"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (76420-384-01)", "package_ndc": "76420-384-01", "marketing_start_date": "20250331"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (76420-384-20)", "package_ndc": "76420-384-20", "marketing_start_date": "20250331"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (76420-384-30)", "package_ndc": "76420-384-30", "marketing_start_date": "20250331"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (76420-384-60)", "package_ndc": "76420-384-60", "marketing_start_date": "20250331"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (76420-384-90)", "package_ndc": "76420-384-90", "marketing_start_date": "20250331"}], "brand_name": "Propranolol Hydrochloride", "product_id": "76420-384_366b6b94-8ad2-8ec9-e063-6394a90a813b", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "76420-384", "generic_name": "Propranolol Hydrochloride", "labeler_name": "Asclemed USA, 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": "20191031", "listing_expiration_date": "20261231"}