Package 71335-2315-1

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2315-1
Digits Only 7133523151
Product NDC 71335-2315
Product ID 71335-2315_d29ee62f-3e89-4501-b241-2f01003a79f5
Description

100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2315-1)

Marketing

Marketing Status
Marketed Since 2023-11-30
Brand propranolol hydrochloride
Generic propranolol hydrochloride
Sample Package No

Linked Drug Pages (1)

propranolol hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d29ee62f-3e89-4501-b241-2f01003a79f5", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856569"], "spl_set_id": ["4803b5bf-8ca4-4a8b-bd24-1f3ff7d93d7e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2315-1)", "package_ndc": "71335-2315-1", "marketing_start_date": "20231130"}], "brand_name": "propranolol hydrochloride", "product_id": "71335-2315_d29ee62f-3e89-4501-b241-2f01003a79f5", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71335-2315", "generic_name": "propranolol hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "propranolol hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA078703", "marketing_category": "ANDA", "marketing_start_date": "20130311", "listing_expiration_date": "20261231"}