metoprolol tartrate

Generic: metoprolol

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

Drug Facts

Product Profile

Brand Name metoprolol tartrate
Generic Name metoprolol
Labeler alembic pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

metoprolol tartrate 25 mg/1

Manufacturer
Alembic Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 62332-112
Product ID 62332-112_c7738f42-299e-4bea-af50-778e069352f0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202871
Listing Expiration 2026-12-31
Marketing Start 2016-07-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62332112
Hyphenated Format 62332-112

Supplemental Identifiers

RxCUI
866511 866514 866924
UPC
0362332113309 0362332114306 0362332112302
UNII
W5S57Y3A5L

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 tartrate (source: ndc)
Generic Name metoprolol (source: ndc)
Application Number ANDA202871 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (62332-112-30)
  • 100 TABLET in 1 BOTTLE (62332-112-31)
  • 1000 TABLET in 1 BOTTLE (62332-112-91)
source: ndc

Packages (3)

Ingredients (1)

metoprolol tartrate (25 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c7738f42-299e-4bea-af50-778e069352f0", "openfda": {"upc": ["0362332113309", "0362332114306", "0362332112302"], "unii": ["W5S57Y3A5L"], "rxcui": ["866511", "866514", "866924"], "spl_set_id": ["24837d82-0f3f-4482-9af0-31e5f675c30f"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (62332-112-30)", "package_ndc": "62332-112-30", "marketing_start_date": "20160731"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (62332-112-31)", "package_ndc": "62332-112-31", "marketing_start_date": "20160731"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (62332-112-91)", "package_ndc": "62332-112-91", "marketing_start_date": "20160731"}], "brand_name": "METOPROLOL TARTRATE", "product_id": "62332-112_c7738f42-299e-4bea-af50-778e069352f0", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "62332-112", "generic_name": "METOPROLOL", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METOPROLOL TARTRATE", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "25 mg/1"}], "application_number": "ANDA202871", "marketing_category": "ANDA", "marketing_start_date": "20160731", "listing_expiration_date": "20261231"}