metoprolol tartrate

Generic: metoprolol

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

Drug Facts

Product Profile

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

metoprolol tartrate 100 mg/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3942
Product ID 68071-3942_47d11563-2d6a-623f-e063-6294a90a54c3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202871
Listing Expiration 2027-12-31
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 680713942
Hyphenated Format 68071-3942

Supplemental Identifiers

RxCUI
866511
UPC
0368071394238
UNII
W5S57Y3A5L

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
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (68071-3942-3)
source: ndc

Packages (1)

68071-3942-3 30 TABLET in 1 BOTTLE (68071-3942-3)

Ingredients (1)

metoprolol tartrate (100 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": "47d11563-2d6a-623f-e063-6294a90a54c3", "openfda": {"upc": ["0368071394238"], "unii": ["W5S57Y3A5L"], "rxcui": ["866511"], "spl_set_id": ["47d11c0c-82dd-33b1-e063-6394a90a6a97"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3942-3)", "package_ndc": "68071-3942-3", "marketing_start_date": "20260107"}], "brand_name": "METOPROLOL TARTRATE", "product_id": "68071-3942_47d11563-2d6a-623f-e063-6294a90a54c3", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68071-3942", "generic_name": "METOPROLOL", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METOPROLOL TARTRATE", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "100 mg/1"}], "application_number": "ANDA202871", "marketing_category": "ANDA", "marketing_start_date": "20160731", "listing_expiration_date": "20271231"}