metoprolol succinate

Generic: metoprolol succinate

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

Drug Facts

Product Profile

Brand Name metoprolol succinate
Generic Name metoprolol succinate
Labeler remedyrepack inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metoprolol succinate 50 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-3164
Product ID 70518-3164_3a21db68-7b93-76d7-e063-6294a90a7c30
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203894
Listing Expiration 2026-12-31
Marketing Start 2021-07-20

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705183164
Hyphenated Format 70518-3164

Supplemental Identifiers

RxCUI
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 ANDA203894 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3164-0)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3164-1)
source: ndc

Packages (2)

70518-3164-0 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3164-0) 70518-3164-1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3164-1)

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": "3a21db68-7b93-76d7-e063-6294a90a7c30", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866436"], "spl_set_id": ["eea82ccb-876b-4fe8-9270-dcea509029a5"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3164-0)", "package_ndc": "70518-3164-0", "marketing_start_date": "20210720"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3164-1)", "package_ndc": "70518-3164-1", "marketing_start_date": "20211005"}], "brand_name": "metoprolol succinate", "product_id": "70518-3164_3a21db68-7b93-76d7-e063-6294a90a7c30", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-3164", "generic_name": "metoprolol succinate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "metoprolol succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA203894", "marketing_category": "ANDA", "marketing_start_date": "20210720", "listing_expiration_date": "20261231"}