metoprolol succinate

Generic: metoprolol succinate

Labeler: granules pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

metoprolol succinate 100 mg/1

Manufacturer
Granules Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 70010-782
Product ID 70010-782_1c7ab139-2fb1-f011-e063-6394a90add6c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216916
Listing Expiration 2026-12-31
Marketing Start 2023-10-02

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70010782
Hyphenated Format 70010-782

Supplemental Identifiers

RxCUI
866412 866419 866427 866436
UPC
0370010782013 0370010783010 0370010781016
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 ANDA216916 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-782-01)
  • 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-782-05)
  • 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-782-10)
source: ndc

Packages (3)

70010-782-01 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-782-01) 70010-782-05 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-782-05) 70010-782-10 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-782-10)

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": "1c7ab139-2fb1-f011-e063-6394a90add6c", "openfda": {"upc": ["0370010782013", "0370010783010", "0370010781016"], "unii": ["TH25PD4CCB"], "rxcui": ["866412", "866419", "866427", "866436"], "spl_set_id": ["ff180ca2-7490-a571-e053-6394a90a97b1"], "manufacturer_name": ["Granules Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-782-01)", "package_ndc": "70010-782-01", "marketing_start_date": "20231002"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-782-05)", "package_ndc": "70010-782-05", "marketing_start_date": "20231002"}, {"sample": false, "description": "1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-782-10)", "package_ndc": "70010-782-10", "marketing_start_date": "20231002"}], "brand_name": "Metoprolol Succinate", "product_id": "70010-782_1c7ab139-2fb1-f011-e063-6394a90add6c", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70010-782", "generic_name": "Metoprolol Succinate", "labeler_name": "Granules Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "100 mg/1"}], "application_number": "ANDA216916", "marketing_category": "ANDA", "marketing_start_date": "20231002", "listing_expiration_date": "20261231"}