metoprolol tartrate
Generic: metoprolol tartrate
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
metoprolol tartrate
Generic Name
metoprolol tartrate
Labeler
a-s medication solutions
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
metoprolol tartrate 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-6084
Product ID
50090-6084_e30144a0-cbaa-40cd-bc5b-24a753c66545
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA200981
Listing Expiration
2026-12-31
Marketing Start
2018-12-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500906084
Hyphenated Format
50090-6084
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
- 50 mg/1
Packaging
- 90 TABLET, FILM COATED in 1 BOTTLE (50090-6084-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e30144a0-cbaa-40cd-bc5b-24a753c66545", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866514"], "spl_set_id": ["56b1de7b-3246-4a5e-a9a1-8970397e901c"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6084-0)", "package_ndc": "50090-6084-0", "marketing_start_date": "20220920"}], "brand_name": "Metoprolol Tartrate", "product_id": "50090-6084_e30144a0-cbaa-40cd-bc5b-24a753c66545", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-6084", "generic_name": "Metoprolol Tartrate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Tartrate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "50 mg/1"}], "application_number": "ANDA200981", "marketing_category": "ANDA", "marketing_start_date": "20181201", "listing_expiration_date": "20261231"}