metoprolol succinate er
Generic: metoprolol succinate
Labeler: direct_rxDrug Facts
Product Profile
Brand Name
metoprolol succinate er
Generic Name
metoprolol succinate
Labeler
direct_rx
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
metoprolol succinate 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
61919-754
Product ID
61919-754_0e993203-3e65-5fbd-e063-6294a90a0636
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204106
Listing Expiration
2026-12-31
Marketing Start
2019-05-02
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
61919754
Hyphenated Format
61919-754
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 succinate er (source: ndc)
Generic Name
metoprolol succinate (source: ndc)
Application Number
ANDA204106 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-754-30)
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-754-90)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0e993203-3e65-5fbd-e063-6294a90a0636", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866412", "866427"], "spl_set_id": ["7ea78d2a-aa9f-38d4-e053-2991aa0a07fe"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-754-30)", "package_ndc": "61919-754-30", "marketing_start_date": "20190502"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-754-90)", "package_ndc": "61919-754-90", "marketing_start_date": "20190502"}], "brand_name": "METOPROLOL SUCCINATE ER", "product_id": "61919-754_0e993203-3e65-5fbd-e063-6294a90a0636", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "61919-754", "generic_name": "METOPROLOL SUCCINATE", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METOPROLOL SUCCINATE", "brand_name_suffix": "ER", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "25 mg/1"}], "application_number": "ANDA204106", "marketing_category": "ANDA", "marketing_start_date": "20190502", "listing_expiration_date": "20261231"}