metoprolol succinate

Generic: metoprolol succinate

Labeler: sun pharmaceutical industries inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol succinate
Generic Name metoprolol succinate
Labeler sun pharmaceutical industries inc.
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metoprolol succinate 100 mg/1

Manufacturer
Sun Pharmaceutical Industries Inc.

Identifiers & Regulatory

Product NDC 63304-010
Product ID 63304-010_32a6b020-3673-469f-8757-741297fb458b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA210428
Listing Expiration 2026-12-31
Marketing Start 2018-02-07

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63304010
Hyphenated Format 63304-010

Supplemental Identifiers

RxCUI
1999031 1999033 1999035 1999037
UPC
0363304010305
UNII
TH25PD4CCB

Packaging Origin

Original Packager
true

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 NDA210428 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63304-010-30)
source: ndc

Packages (1)

Ingredients (1)

metoprolol succinate (100 mg/1)

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 (63304-010-30)", "package_ndc": "63304-010-30", "marketing_start_date": "20180207"}], "brand_name": "Metoprolol Succinate", "product_id": "63304-010_32a6b020-3673-469f-8757-741297fb458b", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "63304-010", "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": "100 mg/1"}], "application_number": "NDA210428", "marketing_category": "NDA", "marketing_start_date": "20180207", "listing_expiration_date": "20261231"}