metoprolol succinate

Generic: metoprolol succinate

Labeler: slate run pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol succinate
Generic Name metoprolol succinate
Labeler slate run pharmaceuticals, llc
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metoprolol succinate 25 mg/1

Manufacturer
Slate Run Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 70436-202
Product ID 70436-202_18a2b62c-c586-60fd-e063-6294a90a2a02
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213854
Listing Expiration 2026-12-31
Marketing Start 2022-10-28

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70436202
Hyphenated Format 70436-202

Supplemental Identifiers

RxCUI
866412 866419 866427 866436
UPC
0370436167012 0370436166022 0370436202034 0370436166015 0370436183012 0370436202027 0370436167029 0370436202010 0370436183036 0370436167036 0370436166039 0370436183029
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 ANDA213854 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-202-01)
  • 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-202-02)
  • 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-202-03)
source: ndc

Packages (3)

70436-202-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-202-01) 70436-202-02 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-202-02) 70436-202-03 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-202-03)

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": "18a2b62c-c586-60fd-e063-6294a90a2a02", "openfda": {"upc": ["0370436167012", "0370436166022", "0370436202034", "0370436166015", "0370436183012", "0370436202027", "0370436167029", "0370436202010", "0370436183036", "0370436167036", "0370436166039", "0370436183029"], "unii": ["TH25PD4CCB"], "rxcui": ["866412", "866419", "866427", "866436"], "spl_set_id": ["c00f99e2-7a88-6f9b-e053-2995a90a6ace"], "manufacturer_name": ["Slate Run Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-202-01)", "package_ndc": "70436-202-01", "marketing_start_date": "20221028"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-202-02)", "package_ndc": "70436-202-02", "marketing_start_date": "20221028"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-202-03)", "package_ndc": "70436-202-03", "marketing_start_date": "20221028"}], "brand_name": "Metoprolol succinate", "product_id": "70436-202_18a2b62c-c586-60fd-e063-6294a90a2a02", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70436-202", "generic_name": "Metoprolol succinate", "labeler_name": "Slate Run Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "25 mg/1"}], "application_number": "ANDA213854", "marketing_category": "ANDA", "marketing_start_date": "20221028", "listing_expiration_date": "20261231"}