metoprolol succinate

Generic: metoprolol succinate

Labeler: zydus lifesciences limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol succinate
Generic Name metoprolol succinate
Labeler zydus lifesciences limited
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metoprolol succinate 25 mg/1

Manufacturer
Zydus Lifesciences Limited

Identifiers & Regulatory

Product NDC 70771-1338
Product ID 70771-1338_1d2d649d-220d-4565-87ad-09f9a4ce8d59
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203894
Listing Expiration 2026-12-31
Marketing Start 2018-06-07

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 707711338
Hyphenated Format 70771-1338

Supplemental Identifiers

RxCUI
866412 866419 866427 866436
UPC
0368382566010 0368382564016 0368382565013 0368382567017
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 ANDA203894 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1338-0)
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1338-1)
  • 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1338-5)
source: ndc

Packages (3)

70771-1338-0 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1338-0) 70771-1338-1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1338-1) 70771-1338-5 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1338-5)

Ingredients (1)

metoprolol succinate (25 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": "1d2d649d-220d-4565-87ad-09f9a4ce8d59", "openfda": {"upc": ["0368382566010", "0368382564016", "0368382565013", "0368382567017"], "unii": ["TH25PD4CCB"], "rxcui": ["866412", "866419", "866427", "866436"], "spl_set_id": ["1098f26d-8319-4dba-ad66-3df22db2b399"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1338-0)", "package_ndc": "70771-1338-0", "marketing_start_date": "20180607"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1338-1)", "package_ndc": "70771-1338-1", "marketing_start_date": "20180607"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1338-5)", "package_ndc": "70771-1338-5", "marketing_start_date": "20180607"}], "brand_name": "metoprolol succinate", "product_id": "70771-1338_1d2d649d-220d-4565-87ad-09f9a4ce8d59", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70771-1338", "generic_name": "metoprolol succinate", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "metoprolol succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "25 mg/1"}], "application_number": "ANDA203894", "marketing_category": "ANDA", "marketing_start_date": "20180607", "listing_expiration_date": "20261231"}