nebivolol

Generic: nebivolol

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nebivolol
Generic Name nebivolol
Labeler direct_rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

nebivolol 20 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-592
Product ID 72189-592_25b5631c-44a4-05b4-e063-6394a90aeb7d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212682
Listing Expiration 2026-12-31
Marketing Start 2024-10-30

Pharmacologic Class

Established (EPC)
beta-adrenergic blocker [epc]
Mechanism of Action
adrenergic beta-antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189592
Hyphenated Format 72189-592

Supplemental Identifiers

RxCUI
827073
UNII
030Y90569U
NUI
N0000000161 N0000175556

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 nebivolol (source: ndc)
Generic Name nebivolol (source: ndc)
Application Number ANDA212682 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (72189-592-60)
source: ndc

Packages (1)

72189-592-60 60 TABLET in 1 BOTTLE (72189-592-60)

Ingredients (1)

nebivolol (20 mg/1)

Linked Drug Pages (1)

Nebivolol ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "25b5631c-44a4-05b4-e063-6394a90aeb7d", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["030Y90569U"], "rxcui": ["827073"], "spl_set_id": ["25b5631c-44a3-05b4-e063-6394a90aeb7d"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (72189-592-60)", "package_ndc": "72189-592-60", "marketing_start_date": "20241030"}], "brand_name": "Nebivolol", "product_id": "72189-592_25b5631c-44a4-05b4-e063-6394a90aeb7d", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72189-592", "generic_name": "Nebivolol", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol", "active_ingredients": [{"name": "NEBIVOLOL", "strength": "20 mg/1"}], "application_number": "ANDA212682", "marketing_category": "ANDA", "marketing_start_date": "20241030", "listing_expiration_date": "20261231"}