metoprolol succinate

Generic: metoprolol succinate

Labeler: zydus pharmaceuticals (usa) inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol succinate
Generic Name metoprolol succinate
Labeler zydus pharmaceuticals (usa) inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metoprolol succinate 100 mg/1

Manufacturer
Zydus Pharmaceuticals (USA) Inc.

Identifiers & Regulatory

Product NDC 68382-566
Product ID 68382-566_0d89802b-2784-4eeb-977c-299ab20fd53e
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 68382566
Hyphenated Format 68382-566

Supplemental Identifiers

RxCUI
866412 866419 866427 866436
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
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-566-01)
  • 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-566-05)
  • 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-566-10)
source: ndc

Packages (3)

68382-566-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-566-01) 68382-566-05 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-566-05) 68382-566-10 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-566-10)

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": "0d89802b-2784-4eeb-977c-299ab20fd53e", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866412", "866419", "866427", "866436"], "spl_set_id": ["bd77ec6e-c58c-440b-81d6-8a462b2fdc9c"], "manufacturer_name": ["Zydus Pharmaceuticals (USA) Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-566-01)", "package_ndc": "68382-566-01", "marketing_start_date": "20180607"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-566-05)", "package_ndc": "68382-566-05", "marketing_start_date": "20180607"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-566-10)", "package_ndc": "68382-566-10", "marketing_start_date": "20180607"}], "brand_name": "metoprolol succinate", "product_id": "68382-566_0d89802b-2784-4eeb-977c-299ab20fd53e", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68382-566", "generic_name": "metoprolol succinate", "labeler_name": "Zydus Pharmaceuticals (USA) Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "metoprolol succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "100 mg/1"}], "application_number": "ANDA203894", "marketing_category": "ANDA", "marketing_start_date": "20180607", "listing_expiration_date": "20261231"}