metoprolol tartrate

Generic: metoprolol

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

Drug Facts

Product Profile

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

metoprolol tartrate 25 mg/1

Manufacturer
Alembic Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 46708-290
Product ID 46708-290_f31d2aef-f902-4984-803c-5bdb015e9253
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202871
Listing Expiration 2026-12-31
Marketing Start 2013-07-22

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 46708290
Hyphenated Format 46708-290

Supplemental Identifiers

RxCUI
866511 866514 866924
UPC
0346708292300 0346708291303 0346708290306
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
  • 100 TABLET in 1 CARTON (46708-290-10)
  • 30 TABLET in 1 BOTTLE (46708-290-30)
  • 100 TABLET in 1 BOTTLE (46708-290-31)
  • 500 TABLET in 1 BOTTLE (46708-290-71)
  • 1000 TABLET in 1 BOTTLE (46708-290-91)
source: ndc

Packages (5)

46708-290-10 100 TABLET in 1 CARTON (46708-290-10) 46708-290-30 30 TABLET in 1 BOTTLE (46708-290-30) 46708-290-31 100 TABLET in 1 BOTTLE (46708-290-31) 46708-290-71 500 TABLET in 1 BOTTLE (46708-290-71) 46708-290-91 1000 TABLET in 1 BOTTLE (46708-290-91)

Ingredients (1)

metoprolol tartrate (25 mg/1)

Linked Drug Pages (1)

METOPROLOL TARTRATE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f31d2aef-f902-4984-803c-5bdb015e9253", "openfda": {"upc": ["0346708292300", "0346708291303", "0346708290306"], "unii": ["W5S57Y3A5L"], "rxcui": ["866511", "866514", "866924"], "spl_set_id": ["cb76a73f-549a-4170-b96a-f93ed7e09464"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 CARTON (46708-290-10)", "package_ndc": "46708-290-10", "marketing_start_date": "20130722"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (46708-290-30)", "package_ndc": "46708-290-30", "marketing_start_date": "20130722"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (46708-290-31)", "package_ndc": "46708-290-31", "marketing_start_date": "20130722"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (46708-290-71)", "package_ndc": "46708-290-71", "marketing_start_date": "20130722"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (46708-290-91)", "package_ndc": "46708-290-91", "marketing_start_date": "20130722"}], "brand_name": "METOPROLOL TARTRATE", "product_id": "46708-290_f31d2aef-f902-4984-803c-5bdb015e9253", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "46708-290", "generic_name": "METOPROLOL", "labeler_name": "Alembic Pharmaceuticals Limited", "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": "20130722", "listing_expiration_date": "20261231"}