nebivolol

Generic: nebivolol

Labeler: cadila pharmaceuticals limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nebivolol
Generic Name nebivolol
Labeler cadila pharmaceuticals limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

nebivolol hydrochloride 20 mg/1

Manufacturer
Cadila Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 71209-061
Product ID 71209-061_0ab335f1-2089-496b-b65f-02c697f6ee89
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208717
Listing Expiration 2026-12-31
Marketing Start 2017-12-29

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71209061
Hyphenated Format 71209-061

Supplemental Identifiers

RxCUI
387013 751612 751618 827073
UPC
0371209060042 0371209060059 0371209058056
UNII
JGS34J7L9I

Packaging Origin

Original Packager
true

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 ANDA208717 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71209-061-01)
  • 90 TABLET in 1 BOTTLE (71209-061-04)
  • 100 TABLET in 1 BOTTLE (71209-061-05)
  • 1000 TABLET in 1 BOTTLE (71209-061-11)
source: ndc

Packages (4)

71209-061-01 30 TABLET in 1 BOTTLE (71209-061-01) 71209-061-04 90 TABLET in 1 BOTTLE (71209-061-04) 71209-061-05 100 TABLET in 1 BOTTLE (71209-061-05) 71209-061-11 1000 TABLET in 1 BOTTLE (71209-061-11)

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": "0ab335f1-2089-496b-b65f-02c697f6ee89", "openfda": {"upc": ["0371209060042", "0371209060059", "0371209058056"], "unii": ["JGS34J7L9I"], "rxcui": ["387013", "751612", "751618", "827073"], "spl_set_id": ["451cdd6e-13b4-402f-8a44-cdf5f7433a49"], "manufacturer_name": ["Cadila Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71209-061-01)", "package_ndc": "71209-061-01", "marketing_start_date": "20181016"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71209-061-04)", "package_ndc": "71209-061-04", "marketing_start_date": "20181016"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71209-061-05)", "package_ndc": "71209-061-05", "marketing_start_date": "20181016"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (71209-061-11)", "package_ndc": "71209-061-11", "marketing_start_date": "20181016"}], "brand_name": "Nebivolol", "product_id": "71209-061_0ab335f1-2089-496b-b65f-02c697f6ee89", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71209-061", "generic_name": "Nebivolol", "labeler_name": "Cadila Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA208717", "marketing_category": "ANDA", "marketing_start_date": "20171229", "listing_expiration_date": "20261231"}