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 2.5 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5708
Product ID 50090-5708_980722af-2bc3-492d-a8ff-835f3b69dd19
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203828
Listing Expiration 2026-12-31
Marketing Start 2021-09-16

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500905708
Hyphenated Format 50090-5708

Supplemental Identifiers

RxCUI
751618
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 ANDA203828 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 5 TABLET in 1 BOTTLE (50090-5708-0)
  • 90 TABLET in 1 BOTTLE (50090-5708-1)
source: ndc

Packages (2)

50090-5708-0 5 TABLET in 1 BOTTLE (50090-5708-0) 50090-5708-1 90 TABLET in 1 BOTTLE (50090-5708-1)

Ingredients (1)

nebivolol hydrochloride (2.5 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": "980722af-2bc3-492d-a8ff-835f3b69dd19", "openfda": {"unii": ["JGS34J7L9I"], "rxcui": ["751618"], "spl_set_id": ["5953f23b-2f41-4b49-bcdb-1691f4ffa35f"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "5 TABLET in 1 BOTTLE (50090-5708-0)", "package_ndc": "50090-5708-0", "marketing_start_date": "20210923"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-5708-1)", "package_ndc": "50090-5708-1", "marketing_start_date": "20211007"}], "brand_name": "Nebivolol", "product_id": "50090-5708_980722af-2bc3-492d-a8ff-835f3b69dd19", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-5708", "generic_name": "Nebivolol", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA203828", "marketing_category": "ANDA", "marketing_start_date": "20210916", "listing_expiration_date": "20261231"}