Package 68071-2522-1
Brand: metoprolol succinate
Generic: metoprolol succinatePackage Facts
Identity
Package NDC
68071-2522-1
Digits Only
6807125221
Product NDC
68071-2522
Description
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-2522-1)
Marketing
Marketing Status
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": "1e79cefa-a416-38b6-e063-6394a90a5eb8", "openfda": {"upc": ["0368071252217"], "unii": ["TH25PD4CCB"], "rxcui": ["866436"], "spl_set_id": ["ca8dbdc1-0137-8a89-e053-2995a90a66fd"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-2522-1)", "package_ndc": "68071-2522-1", "marketing_start_date": "20210827"}], "brand_name": "metoprolol succinate", "product_id": "68071-2522_1e79cefa-a416-38b6-e063-6394a90a5eb8", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68071-2522", "generic_name": "metoprolol succinate", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "metoprolol succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA203894", "marketing_category": "ANDA", "marketing_start_date": "20180607", "listing_expiration_date": "20261231"}