metoprolol succinate

Generic: metoprolol succinate

Labeler: legacy pharmaceutical packaging, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol succinate
Generic Name metoprolol succinate
Labeler legacy pharmaceutical packaging, llc
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metoprolol succinate 50 mg/1

Manufacturer
Legacy Pharmaceutical Packaging, LLC

Identifiers & Regulatory

Product NDC 68645-478
Product ID 68645-478_9732391a-6668-4cbe-96ac-575496e378e0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090617
Listing Expiration 2027-12-31
Marketing Start 2012-09-10

Pharmacologic Class

Classes
adrenergic beta-antagonists [moa] beta-adrenergic blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68645478
Hyphenated Format 68645-478

Supplemental Identifiers

RxCUI
866427 866436
UPC
0368645478548 0368645477541
UNII
TH25PD4CCB

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name metoprolol succinate (source: ndc)
Generic Name metoprolol succinate (source: ndc)
Application Number ANDA090617 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68645-478-54)
source: ndc

Packages (1)

68645-478-54 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68645-478-54)

Ingredients (1)

metoprolol succinate (50 mg/1)

Linked Drug Pages (1)

Metoprolol succinate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9732391a-6668-4cbe-96ac-575496e378e0", "openfda": {"upc": ["0368645478548", "0368645477541"], "unii": ["TH25PD4CCB"], "rxcui": ["866427", "866436"], "spl_set_id": ["98d31d43-eff0-4ba9-9953-f2f53c13b3d9"], "manufacturer_name": ["Legacy Pharmaceutical Packaging, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68645-478-54)", "package_ndc": "68645-478-54", "marketing_start_date": "20120910"}], "brand_name": "Metoprolol succinate", "product_id": "68645-478_9732391a-6668-4cbe-96ac-575496e378e0", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68645-478", "generic_name": "Metoprolol succinate", "labeler_name": "Legacy Pharmaceutical Packaging, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA090617", "marketing_category": "ANDA", "marketing_start_date": "20120910", "listing_expiration_date": "20271231"}