metoprolol succinate

Generic: metoprolol succinate

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol succinate
Generic Name metoprolol succinate
Labeler major pharmaceuticals
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metoprolol succinate 50 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-6323
Product ID 0904-6323_14987ae1-e9df-4f1f-8887-c67e4ca1a218
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090617
Listing Expiration 2026-12-31
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 09046323
Hyphenated Format 0904-6323

Supplemental Identifiers

RxCUI
866427 866436
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
  • 100 BLISTER PACK in 1 CARTON (0904-6323-61) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
source: ndc

Packages (1)

0904-6323-61 100 BLISTER PACK in 1 CARTON (0904-6323-61) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

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": "14987ae1-e9df-4f1f-8887-c67e4ca1a218", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866427", "866436"], "spl_set_id": ["14ab9921-4651-4abc-92dc-aab1719b6bb0"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6323-61)  / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "0904-6323-61", "marketing_start_date": "20120910"}], "brand_name": "Metoprolol succinate", "product_id": "0904-6323_14987ae1-e9df-4f1f-8887-c67e4ca1a218", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0904-6323", "generic_name": "Metoprolol succinate", "labeler_name": "Major Pharmaceuticals", "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": "20261231"}