metoprolol succinate

Generic: metoprolol succinate

Labeler: dr. reddy's laboratories limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol succinate
Generic Name metoprolol succinate
Labeler dr. reddy's laboratories limited
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metoprolol succinate 200 mg/1

Manufacturer
Dr. Reddy's Laboratories Limited

Identifiers & Regulatory

Product NDC 55111-469
Product ID 55111-469_24d7f7ba-6db9-f2f2-fb99-9568f65cd9be
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078889
Listing Expiration 2026-12-31
Marketing Start 2012-09-10

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55111469
Hyphenated Format 55111-469

Supplemental Identifiers

RxCUI
866412 866419
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 ANDA078889 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-469-01)
  • 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-469-05)
  • 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-469-30)
  • 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-469-60)
  • 10 BLISTER PACK in 1 CARTON (55111-469-78) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (55111-469-79)
source: ndc

Packages (5)

Ingredients (1)

metoprolol succinate (200 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "24d7f7ba-6db9-f2f2-fb99-9568f65cd9be", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866412", "866419"], "spl_set_id": ["71c1d33e-be6f-6d59-b715-45075445891a"], "manufacturer_name": ["Dr. Reddy's Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-469-01)", "package_ndc": "55111-469-01", "marketing_start_date": "20120910"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-469-05)", "package_ndc": "55111-469-05", "marketing_start_date": "20120910"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-469-30)", "package_ndc": "55111-469-30", "marketing_start_date": "20120910"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-469-60)", "package_ndc": "55111-469-60", "marketing_start_date": "20120910"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (55111-469-78)  / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (55111-469-79)", "package_ndc": "55111-469-78", "marketing_start_date": "20120910"}], "brand_name": "Metoprolol succinate", "product_id": "55111-469_24d7f7ba-6db9-f2f2-fb99-9568f65cd9be", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "55111-469", "generic_name": "Metoprolol succinate", "labeler_name": "Dr. Reddy's Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "200 mg/1"}], "application_number": "ANDA078889", "marketing_category": "ANDA", "marketing_start_date": "20120910", "listing_expiration_date": "20261231"}