metoprolol succinate

Generic: metoprolol succinate

Labeler: granules india ltd
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol succinate
Generic Name metoprolol succinate
Labeler granules india ltd
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metoprolol succinate 100 mg/1

Manufacturer
Granules India Ltd

Identifiers & Regulatory

Product NDC 62207-131
Product ID 62207-131_327de2c2-8091-50cc-e063-6394a90a14d2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216509
Listing Expiration 2026-12-31
Marketing Start 2024-08-16

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62207131
Hyphenated Format 62207-131

Supplemental Identifiers

RxCUI
866412 866419 866427 866436
UPC
0362207133548 0362207130547 0362207132541
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 ANDA216509 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (62207-131-49)
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62207-131-54)
source: ndc

Packages (2)

62207-131-49 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (62207-131-49) 62207-131-54 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62207-131-54)

Ingredients (1)

metoprolol succinate (100 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": "327de2c2-8091-50cc-e063-6394a90a14d2", "openfda": {"upc": ["0362207133548", "0362207130547", "0362207132541"], "unii": ["TH25PD4CCB"], "rxcui": ["866412", "866419", "866427", "866436"], "spl_set_id": ["c5431c8a-d92c-489e-b63b-4b9cc8f32a1a"], "manufacturer_name": ["Granules India Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (62207-131-49)", "package_ndc": "62207-131-49", "marketing_start_date": "20240816"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62207-131-54)", "package_ndc": "62207-131-54", "marketing_start_date": "20240816"}], "brand_name": "Metoprolol Succinate", "product_id": "62207-131_327de2c2-8091-50cc-e063-6394a90a14d2", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "62207-131", "generic_name": "Metoprolol Succinate", "labeler_name": "Granules India Ltd", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "100 mg/1"}], "application_number": "ANDA216509", "marketing_category": "ANDA", "marketing_start_date": "20240816", "listing_expiration_date": "20261231"}