Package 50090-7263-0
Brand: propranolol hydrochloride
Generic: propranolol hydrochloridePackage Facts
Identity
Package NDC
50090-7263-0
Digits Only
5009072630
Product NDC
50090-7263
Description
30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-7263-0)
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": "152ccf8d-9d06-4ba2-bc76-ae5b11579d47", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856569"], "spl_set_id": ["87967c3a-4a6e-45c8-ae3d-1e1dbaa4ba10"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-7263-0)", "package_ndc": "50090-7263-0", "marketing_start_date": "20241003"}], "brand_name": "Propranolol Hydrochloride", "product_id": "50090-7263_152ccf8d-9d06-4ba2-bc76-ae5b11579d47", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-7263", "generic_name": "propranolol hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA212026", "marketing_category": "ANDA", "marketing_start_date": "20200106", "listing_expiration_date": "20261231"}