nebivolol

Generic: nebivolol

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nebivolol
Generic Name nebivolol
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

nebivolol 20 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7301
Product ID 50090-7301_0b07851d-3512-4549-b39b-194211f6946f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212682
Listing Expiration 2026-12-31
Marketing Start 2022-02-14

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 500907301
Hyphenated Format 50090-7301

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
  • 30 TABLET in 1 BOTTLE (50090-7301-1)
  • 90 TABLET in 1 BOTTLE (50090-7301-2)
source: ndc

Packages (2)

50090-7301-1 30 TABLET in 1 BOTTLE (50090-7301-1) 50090-7301-2 90 TABLET in 1 BOTTLE (50090-7301-2)

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": "0b07851d-3512-4549-b39b-194211f6946f", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["030Y90569U"], "rxcui": ["827073"], "spl_set_id": ["f20fda1a-437d-4812-b519-a26684c96c6d"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-7301-1)", "package_ndc": "50090-7301-1", "marketing_start_date": "20241014"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7301-2)", "package_ndc": "50090-7301-2", "marketing_start_date": "20241014"}], "brand_name": "NEBIVOLOL", "product_id": "50090-7301_0b07851d-3512-4549-b39b-194211f6946f", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-7301", "generic_name": "nebivolol", "labeler_name": "A-S Medication Solutions", "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": "20220214", "listing_expiration_date": "20261231"}