carvedilol

Generic: carvedilol

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name carvedilol
Generic Name carvedilol
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

carvedilol 25 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-440
Product ID 72789-440_41d761af-3186-eaae-e063-6394a90a7687
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078165
Listing Expiration 2026-12-31
Marketing Start 2021-07-29

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 72789440
Hyphenated Format 72789-440

Supplemental Identifiers

RxCUI
200033
UPC
0372789440934
UNII
0K47UL67F2
NUI
N0000000099 N0000009923 N0000009924 N0000175553 N0000175556

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 ANDA078165 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-440-90)
  • 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-440-93)
source: ndc

Packages (2)

72789-440-90 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-440-90) 72789-440-93 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-440-93)

Ingredients (1)

carvedilol (25 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": "41d761af-3186-eaae-e063-6394a90a7687", "openfda": {"nui": ["N0000000099", "N0000009923", "N0000009924", "N0000175553", "N0000175556"], "upc": ["0372789440934"], "unii": ["0K47UL67F2"], "rxcui": ["200033"], "spl_set_id": ["9959f5d7-c363-4b8d-b8b9-7b45a8cb9aa9"], "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": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-440-90)", "package_ndc": "72789-440-90", "marketing_start_date": "20241104"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-440-93)", "package_ndc": "72789-440-93", "marketing_start_date": "20241011"}], "brand_name": "CARVEDILOL", "product_id": "72789-440_41d761af-3186-eaae-e063-6394a90a7687", "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": "72789-440", "generic_name": "CARVEDILOL", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CARVEDILOL", "active_ingredients": [{"name": "CARVEDILOL", "strength": "25 mg/1"}], "application_number": "ANDA078165", "marketing_category": "ANDA", "marketing_start_date": "20210729", "listing_expiration_date": "20261231"}