carvedilol phosphate

Generic: carvedilol phosphate

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name carvedilol phosphate
Generic Name carvedilol phosphate
Labeler sun pharmaceutical industries, inc.
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

carvedilol phosphate 40 mg/1

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 57664-665
Product ID 57664-665_468e6649-e69b-4938-e063-6394a90ad7a2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090132
Listing Expiration 2026-12-31
Marketing Start 2017-11-08

Pharmacologic Class

Classes
adrenergic alpha-antagonists [moa] adrenergic beta1-antagonists [moa] adrenergic beta2-antagonists [moa] alpha-adrenergic blocker [epc] beta-adrenergic blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 57664665
Hyphenated Format 57664-665

Supplemental Identifiers

RxCUI
860510 860516 860522 860532
UPC
0357664663837 0357664664834 0357664665831 0357664666838
UNII
EQT531S367

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 phosphate (source: ndc)
Generic Name carvedilol phosphate (source: ndc)
Application Number ANDA090132 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (57664-665-83)
source: ndc

Packages (1)

57664-665-83 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (57664-665-83)

Ingredients (1)

carvedilol phosphate (40 mg/1)

Linked Drug Pages (1)

Carvedilol Phosphate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "468e6649-e69b-4938-e063-6394a90ad7a2", "openfda": {"upc": ["0357664663837", "0357664664834", "0357664665831", "0357664666838"], "unii": ["EQT531S367"], "rxcui": ["860510", "860516", "860522", "860532"], "spl_set_id": ["a9314bc0-fd5d-477b-bef5-3bee532774c0"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (57664-665-83)", "package_ndc": "57664-665-83", "marketing_start_date": "20171108"}], "brand_name": "Carvedilol Phosphate", "product_id": "57664-665_468e6649-e69b-4938-e063-6394a90ad7a2", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "Adrenergic beta1-Antagonists [MoA]", "Adrenergic beta2-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "57664-665", "generic_name": "Carvedilol Phosphate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Carvedilol Phosphate", "active_ingredients": [{"name": "CARVEDILOL PHOSPHATE", "strength": "40 mg/1"}], "application_number": "ANDA090132", "marketing_category": "ANDA", "marketing_start_date": "20171108", "listing_expiration_date": "20261231"}