Package 71335-2835-1

Brand: metoprolol succinate

Generic: metoprolol succinate er tablets
NDC Package

Package Facts

Identity

Package NDC 71335-2835-1
Digits Only 7133528351
Product NDC 71335-2835
Product ID 71335-2835_c6fa01d0-4c99-423d-8b61-9c05c44cd355
Description

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2835-1)

Marketing

Marketing Status
Marketed Since 2025-11-10
Brand metoprolol succinate
Generic metoprolol succinate er tablets
Sample Package No

Linked Drug Pages (1)

Metoprolol Succinate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c6fa01d0-4c99-423d-8b61-9c05c44cd355", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866436"], "spl_set_id": ["38429f45-5dc7-4455-840c-dee48f60d95b"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2835-1)", "package_ndc": "71335-2835-1", "marketing_start_date": "20251110"}], "brand_name": "Metoprolol Succinate", "product_id": "71335-2835_c6fa01d0-4c99-423d-8b61-9c05c44cd355", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71335-2835", "generic_name": "Metoprolol Succinate ER Tablets", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA211143", "marketing_category": "ANDA", "marketing_start_date": "20201127", "listing_expiration_date": "20261231"}