metoprolol succinate

Generic: metoprolol succinate

Labeler: dr. reddy's laboratories inc
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 inc
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metoprolol succinate 100 mg/1

Manufacturer
Dr. Reddy's Laboratories Inc

Identifiers & Regulatory

Product NDC 75907-345
Product ID 75907-345_9b4078bf-b309-c50b-d195-b4722dfb0945
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078889
Listing Expiration 2027-12-31
Marketing Start 2026-01-13

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 75907345
Hyphenated Format 75907-345

Supplemental Identifiers

RxCUI
866412 866419
UPC
0375907345012 0375907346019
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
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (75907-345-01)
  • 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (75907-345-10)
source: ndc

Packages (2)

75907-345-01 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (75907-345-01) 75907-345-10 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (75907-345-10)

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": "9b4078bf-b309-c50b-d195-b4722dfb0945", "openfda": {"upc": ["0375907345012", "0375907346019"], "unii": ["TH25PD4CCB"], "rxcui": ["866412", "866419"], "spl_set_id": ["5b7095c8-f8b7-adc7-9052-92325da33a02"], "manufacturer_name": ["Dr. Reddy's Laboratories Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (75907-345-01)", "package_ndc": "75907-345-01", "marketing_start_date": "20260113"}, {"sample": false, "description": "1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (75907-345-10)", "package_ndc": "75907-345-10", "marketing_start_date": "20260113"}], "brand_name": "Metoprolol succinate", "product_id": "75907-345_9b4078bf-b309-c50b-d195-b4722dfb0945", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "75907-345", "generic_name": "Metoprolol succinate", "labeler_name": "Dr. Reddy's Laboratories Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "100 mg/1"}], "application_number": "ANDA078889", "marketing_category": "ANDA", "marketing_start_date": "20260113", "listing_expiration_date": "20271231"}