Package 60760-576-30
Brand: propranolol hydrochloride
Generic: propranolol hydrochloridePackage Facts
Identity
Package NDC
60760-576-30
Digits Only
6076057630
Product NDC
60760-576
Description
30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-576-30)
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": "edc4ccfc-0108-774f-e053-2a95a90a216e", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856569"], "spl_set_id": ["edc4ccfc-0107-774f-e053-2a95a90a216e"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-576-30)", "package_ndc": "60760-576-30", "marketing_start_date": "20221031"}], "brand_name": "Propranolol Hydrochloride", "product_id": "60760-576_edc4ccfc-0108-774f-e053-2a95a90a216e", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "60760-576", "generic_name": "propranolol hydrochloride", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "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": "20221031", "listing_expiration_date": "20261231"}