nebivolol

Generic: nebivolol

Labeler: camber pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nebivolol
Generic Name nebivolol
Labeler camber pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

nebivolol hydrochloride 2.5 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-585
Product ID 31722-585_103af555-44dd-5dfb-e063-6294a90a259f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203825
Listing Expiration 2026-12-31
Marketing Start 2021-09-17

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 31722585
Hyphenated Format 31722-585

Supplemental Identifiers

RxCUI
387013 751612 751618 827073
UPC
0331722585309 0331722588300 0331722587303 0331722586306
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 ANDA203825 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (31722-585-01)
  • 30 TABLET in 1 BOTTLE (31722-585-30)
  • 12 BLISTER PACK in 1 CARTON (31722-585-32) / 10 TABLET in 1 BLISTER PACK (31722-585-31)
  • 15 BLISTER PACK in 1 CARTON (31722-585-34) / 10 TABLET in 1 BLISTER PACK (31722-585-33)
source: ndc

Packages (4)

31722-585-01 100 TABLET in 1 BOTTLE (31722-585-01) 31722-585-30 30 TABLET in 1 BOTTLE (31722-585-30) 31722-585-32 12 BLISTER PACK in 1 CARTON (31722-585-32) / 10 TABLET in 1 BLISTER PACK (31722-585-31) 31722-585-34 15 BLISTER PACK in 1 CARTON (31722-585-34) / 10 TABLET in 1 BLISTER PACK (31722-585-33)

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": "103af555-44dd-5dfb-e063-6294a90a259f", "openfda": {"upc": ["0331722585309", "0331722588300", "0331722587303", "0331722586306"], "unii": ["JGS34J7L9I"], "rxcui": ["387013", "751612", "751618", "827073"], "spl_set_id": ["202d5142-6180-4d48-9a9f-1bd6992fc49b"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (31722-585-01)", "package_ndc": "31722-585-01", "marketing_start_date": "20210917"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (31722-585-30)", "package_ndc": "31722-585-30", "marketing_start_date": "20210917"}, {"sample": false, "description": "12 BLISTER PACK in 1 CARTON (31722-585-32)  / 10 TABLET in 1 BLISTER PACK (31722-585-31)", "package_ndc": "31722-585-32", "marketing_start_date": "20210917"}, {"sample": false, "description": "15 BLISTER PACK in 1 CARTON (31722-585-34)  / 10 TABLET in 1 BLISTER PACK (31722-585-33)", "package_ndc": "31722-585-34", "marketing_start_date": "20210917"}], "brand_name": "Nebivolol", "product_id": "31722-585_103af555-44dd-5dfb-e063-6294a90a259f", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "31722-585", "generic_name": "Nebivolol", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA203825", "marketing_category": "ANDA", "marketing_start_date": "20210917", "listing_expiration_date": "20261231"}