metoprolol succinate

Generic: metoprolol succinate

Labeler: bluepoint laboratories
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol succinate
Generic Name metoprolol succinate
Labeler bluepoint laboratories
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metoprolol succinate 200 mg/1

Manufacturer
BluePoint Laboratories

Identifiers & Regulatory

Product NDC 68001-120
Product ID 68001-120_1aeaf7d4-6a9a-49c8-8e09-6f4411462ee4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078889
Listing Expiration 2026-12-31
Marketing Start 2013-11-25

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68001120
Hyphenated Format 68001-120

Supplemental Identifiers

RxCUI
866412 866419
UPC
0368001119009 0368001120005
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, EXTENDED RELEASE in 1 BOTTLE (68001-120-00)
  • 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-120-03)
source: ndc

Packages (2)

68001-120-00 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-120-00) 68001-120-03 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-120-03)

Ingredients (1)

metoprolol succinate (200 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": "1aeaf7d4-6a9a-49c8-8e09-6f4411462ee4", "openfda": {"upc": ["0368001119009", "0368001120005"], "unii": ["TH25PD4CCB"], "rxcui": ["866412", "866419"], "spl_set_id": ["5ef12832-15cd-40f4-bf11-6cea7e48ff7f"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-120-00)", "package_ndc": "68001-120-00", "marketing_start_date": "20131125"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-120-03)", "package_ndc": "68001-120-03", "marketing_start_date": "20131125"}], "brand_name": "Metoprolol succinate", "product_id": "68001-120_1aeaf7d4-6a9a-49c8-8e09-6f4411462ee4", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68001-120", "generic_name": "Metoprolol succinate", "labeler_name": "BluePoint Laboratories", "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": "20131125", "listing_expiration_date": "20261231"}