metoprolol succinate

Generic: metoprolol succinate er tablets

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

Drug Facts

Product Profile

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

metoprolol succinate 50 mg/1

Manufacturer
BluePoint Laboratories

Identifiers & Regulatory

Product NDC 68001-501
Product ID 68001-501_47e38e34-d590-f7ab-e063-6394a90aa6a3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211143
Listing Expiration 2027-12-31
Marketing Start 2021-05-14

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68001501
Hyphenated Format 68001-501

Supplemental Identifiers

RxCUI
866412 866419 866427 866436
UPC
0368001500005
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 er tablets (source: ndc)
Application Number ANDA211143 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-501-00)
  • 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-501-03)
source: ndc

Packages (2)

68001-501-00 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-501-00) 68001-501-03 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-501-03)

Ingredients (1)

metoprolol succinate (50 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": "47e38e34-d590-f7ab-e063-6394a90aa6a3", "openfda": {"upc": ["0368001500005"], "unii": ["TH25PD4CCB"], "rxcui": ["866412", "866419", "866427", "866436"], "spl_set_id": ["6588d77c-090f-4722-9c91-437887d4624a"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-501-00)", "package_ndc": "68001-501-00", "marketing_start_date": "20210514"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-501-03)", "package_ndc": "68001-501-03", "marketing_start_date": "20210514"}], "brand_name": "Metoprolol Succinate", "product_id": "68001-501_47e38e34-d590-f7ab-e063-6394a90aa6a3", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68001-501", "generic_name": "Metoprolol Succinate ER Tablets", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA211143", "marketing_category": "ANDA", "marketing_start_date": "20210514", "listing_expiration_date": "20271231"}