carvedilol

Generic: carvedilol

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name carvedilol
Generic Name carvedilol
Labeler aurobindo pharma limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

carvedilol 3.125 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 65862-142
Product ID 65862-142_f210723f-29fb-46c7-8ac4-5009d9696d3b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078332
Listing Expiration 2026-12-31
Marketing Start 2007-09-05

Pharmacologic Class

Established (EPC)
alpha-adrenergic blocker [epc] beta-adrenergic blocker [epc]
Mechanism of Action
adrenergic alpha-antagonists [moa] adrenergic beta1-antagonists [moa] adrenergic beta2-antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65862142
Hyphenated Format 65862-142

Supplemental Identifiers

RxCUI
200031 200032 200033 686924
UNII
0K47UL67F2
NUI
N0000000099 N0000009923 N0000009924 N0000175553 N0000175556

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 carvedilol (source: ndc)
Generic Name carvedilol (source: ndc)
Application Number ANDA078332 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 3.125 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (65862-142-01)
  • 500 TABLET, FILM COATED in 1 BOTTLE (65862-142-05)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (65862-142-99)
source: ndc

Packages (3)

65862-142-01 100 TABLET, FILM COATED in 1 BOTTLE (65862-142-01) 65862-142-05 500 TABLET, FILM COATED in 1 BOTTLE (65862-142-05) 65862-142-99 1000 TABLET, FILM COATED in 1 BOTTLE (65862-142-99)

Ingredients (1)

carvedilol (3.125 mg/1)

Linked Drug Pages (1)

Carvedilol ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f210723f-29fb-46c7-8ac4-5009d9696d3b", "openfda": {"nui": ["N0000000099", "N0000009923", "N0000009924", "N0000175553", "N0000175556"], "unii": ["0K47UL67F2"], "rxcui": ["200031", "200032", "200033", "686924"], "spl_set_id": ["7cc14b86-0833-4c3c-91f3-7963d7052fd5"], "pharm_class_epc": ["alpha-Adrenergic Blocker [EPC]", "beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic alpha-Antagonists [MoA]", "Adrenergic beta1-Antagonists [MoA]", "Adrenergic beta2-Antagonists [MoA]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65862-142-01)", "package_ndc": "65862-142-01", "marketing_start_date": "20070905"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (65862-142-05)", "package_ndc": "65862-142-05", "marketing_start_date": "20070905"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65862-142-99)", "package_ndc": "65862-142-99", "marketing_start_date": "20070905"}], "brand_name": "Carvedilol", "product_id": "65862-142_f210723f-29fb-46c7-8ac4-5009d9696d3b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "Adrenergic beta1-Antagonists [MoA]", "Adrenergic beta2-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "65862-142", "generic_name": "Carvedilol", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Carvedilol", "active_ingredients": [{"name": "CARVEDILOL", "strength": "3.125 mg/1"}], "application_number": "ANDA078332", "marketing_category": "ANDA", "marketing_start_date": "20070905", "listing_expiration_date": "20261231"}