metoprolol succinate

Generic: metoprolol succinate

Labeler: camber pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol succinate
Generic Name metoprolol succinate
Labeler camber pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metoprolol succinate 25 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-589
Product ID 31722-589_1376704a-04ff-0a4f-e063-6294a90ae9b8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205541
Listing Expiration 2026-12-31
Marketing Start 2020-11-06

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 31722589
Hyphenated Format 31722-589

Supplemental Identifiers

RxCUI
866412 866419 866427 866436
UPC
0331722591300 0331722592307 0331722590303 0331722589307
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 ANDA205541 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-589-01)
  • 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-589-05)
  • 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-589-10)
  • 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-589-30)
source: ndc

Packages (4)

31722-589-01 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-589-01) 31722-589-05 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-589-05) 31722-589-10 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-589-10) 31722-589-30 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-589-30)

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": "1376704a-04ff-0a4f-e063-6294a90ae9b8", "openfda": {"upc": ["0331722591300", "0331722592307", "0331722590303", "0331722589307"], "unii": ["TH25PD4CCB"], "rxcui": ["866412", "866419", "866427", "866436"], "spl_set_id": ["74a28333-53c1-493e-b6ad-2192fdc35391"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-589-01)", "package_ndc": "31722-589-01", "marketing_start_date": "20201106"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-589-05)", "package_ndc": "31722-589-05", "marketing_start_date": "20210423"}, {"sample": false, "description": "1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-589-10)", "package_ndc": "31722-589-10", "marketing_start_date": "20210423"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-589-30)", "package_ndc": "31722-589-30", "marketing_start_date": "20201106"}], "brand_name": "METOPROLOL SUCCINATE", "product_id": "31722-589_1376704a-04ff-0a4f-e063-6294a90ae9b8", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "31722-589", "generic_name": "METOPROLOL SUCCINATE", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METOPROLOL SUCCINATE", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "25 mg/1"}], "application_number": "ANDA205541", "marketing_category": "ANDA", "marketing_start_date": "20201106", "listing_expiration_date": "20261231"}