Package 63304-008-30

Brand: metoprolol succinate

Generic: metoprolol succinate
NDC Package

Package Facts

Identity

Package NDC 63304-008-30
Digits Only 6330400830
Product NDC 63304-008
Description

30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63304-008-30)

Marketing

Marketing Status
Marketed Since 2018-02-07
Brand metoprolol succinate
Generic metoprolol succinate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "32a6b020-3673-469f-8757-741297fb458b", "openfda": {"upc": ["0363304010305"], "unii": ["TH25PD4CCB"], "rxcui": ["1999031", "1999033", "1999035", "1999037"], "spl_set_id": ["90aa06a3-100f-4466-b950-506303707b01"], "manufacturer_name": ["Sun Pharmaceutical Industries Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63304-008-30)", "package_ndc": "63304-008-30", "marketing_start_date": "20180207"}], "brand_name": "Metoprolol Succinate", "product_id": "63304-008_32a6b020-3673-469f-8757-741297fb458b", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "63304-008", "generic_name": "Metoprolol Succinate", "labeler_name": "Sun Pharmaceutical Industries Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "25 mg/1"}], "application_number": "NDA210428", "marketing_category": "NDA", "marketing_start_date": "20180207", "listing_expiration_date": "20261231"}