metoprolol tartrate
Generic: metoprolol tartrate
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
metoprolol tartrate
Generic Name
metoprolol tartrate
Labeler
remedyrepack inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
metoprolol tartrate 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-3950
Product ID
70518-3950_3b8ce8a9-82a7-30ed-e063-6394a90af92b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA200981
Listing Expiration
2026-12-31
Marketing Start
2023-12-11
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705183950
Hyphenated Format
70518-3950
Supplemental Identifiers
RxCUI
UNII
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 tartrate (source: ndc)
Application Number
ANDA200981 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3950-0)
- 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3950-1)
- 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3950-2)
- 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3950-3)
Packages (4)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3b8ce8a9-82a7-30ed-e063-6394a90af92b", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866924"], "spl_set_id": ["fae7a662-9b27-4c5f-80b5-22442f0ae436"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3950-0)", "package_ndc": "70518-3950-0", "marketing_start_date": "20231211"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3950-1)", "package_ndc": "70518-3950-1", "marketing_start_date": "20231225"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3950-2)", "package_ndc": "70518-3950-2", "marketing_start_date": "20240711"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3950-3)", "package_ndc": "70518-3950-3", "marketing_start_date": "20250731"}], "brand_name": "METOPROLOL TARTRATE", "product_id": "70518-3950_3b8ce8a9-82a7-30ed-e063-6394a90af92b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-3950", "generic_name": "METOPROLOL TARTRATE", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METOPROLOL TARTRATE", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "25 mg/1"}], "application_number": "ANDA200981", "marketing_category": "ANDA", "marketing_start_date": "20231211", "listing_expiration_date": "20261231"}