Package 51655-426-26
Brand: propranolol hydrochloride
Generic: propranolol hydrochloridePackage Facts
Identity
Package NDC
51655-426-26
Digits Only
5165542626
Product NDC
51655-426
Description
90 TABLET in 1 BOTTLE, PLASTIC (51655-426-26)
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": "48ff25f0-9f7d-30f4-e063-6294a90addbc", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856457"], "spl_set_id": ["c29d733a-4fcb-6564-e053-2995a90ae541"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51655-426-26)", "package_ndc": "51655-426-26", "marketing_start_date": "20210114"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-426-52)", "package_ndc": "51655-426-52", "marketing_start_date": "20200827"}], "brand_name": "Propranolol Hydrochloride", "product_id": "51655-426_48ff25f0-9f7d-30f4-e063-6294a90addbc", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "51655-426", "generic_name": "Propranolol Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "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": "20200827", "listing_expiration_date": "20271231"}