metoprolol succinate

Generic: metoprolol succinate

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol succinate
Generic Name metoprolol succinate
Labeler american health packaging
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metoprolol succinate 50 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-402
Product ID 60687-402_22027775-f0b5-c7f5-e063-6394a90a25f6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090617
Listing Expiration 2026-12-31
Marketing Start 2018-12-07

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687402
Hyphenated Format 60687-402

Supplemental Identifiers

RxCUI
866412 866427 866436
UNII
TH25PD4CCB

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 (source: ndc)
Generic Name metoprolol succinate (source: ndc)
Application Number ANDA090617 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-402-01) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-402-11)
  • 50 BLISTER PACK in 1 CARTON (60687-402-65) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-402-11)
source: ndc

Packages (2)

60687-402-01 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-402-01) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-402-11) 60687-402-65 50 BLISTER PACK in 1 CARTON (60687-402-65) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-402-11)

Ingredients (1)

metoprolol succinate (50 mg/1)

Linked Drug Pages (1)

Metoprolol Succinate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "22027775-f0b5-c7f5-e063-6394a90a25f6", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866412", "866427", "866436"], "spl_set_id": ["74e3b4dc-eb30-4d7c-a558-cf58f6470496"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-402-01)  / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-402-11)", "package_ndc": "60687-402-01", "marketing_start_date": "20181207"}, {"sample": false, "description": "50 BLISTER PACK in 1 CARTON (60687-402-65)  / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-402-11)", "package_ndc": "60687-402-65", "marketing_start_date": "20230308"}], "brand_name": "Metoprolol Succinate", "product_id": "60687-402_22027775-f0b5-c7f5-e063-6394a90a25f6", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "60687-402", "generic_name": "Metoprolol Succinate", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA090617", "marketing_category": "ANDA", "marketing_start_date": "20181207", "listing_expiration_date": "20261231"}