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 hydrochloride 20 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7853
Product ID 50090-7853_caccc638-504d-4309-a952-dda8de1f85c1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217397
Listing Expiration 2027-12-31
Marketing Start 2024-10-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907853
Hyphenated Format 50090-7853

Supplemental Identifiers

RxCUI
827073
UNII
JGS34J7L9I

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 ANDA217397 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-7853-1)
  • 90 TABLET in 1 BOTTLE (50090-7853-2)
source: ndc

Packages (2)

50090-7853-1 30 TABLET in 1 BOTTLE (50090-7853-1) 50090-7853-2 90 TABLET in 1 BOTTLE (50090-7853-2)

Ingredients (1)

nebivolol hydrochloride (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": "caccc638-504d-4309-a952-dda8de1f85c1", "openfda": {"unii": ["JGS34J7L9I"], "rxcui": ["827073"], "spl_set_id": ["78c20341-4fbf-4c78-9817-03e7e0072f82"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-7853-1)", "package_ndc": "50090-7853-1", "marketing_start_date": "20260108"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7853-2)", "package_ndc": "50090-7853-2", "marketing_start_date": "20260108"}], "brand_name": "NEBIVOLOL", "product_id": "50090-7853_caccc638-504d-4309-a952-dda8de1f85c1", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-7853", "generic_name": "NEBIVOLOL", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NEBIVOLOL", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA217397", "marketing_category": "ANDA", "marketing_start_date": "20241001", "listing_expiration_date": "20271231"}