carvedilol

Generic: carvedilol

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name carvedilol
Generic Name carvedilol
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

carvedilol 25 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7849
Product ID 50090-7849_fd7346c4-4f59-48ad-a3fd-d64636e10952
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078165
Listing Expiration 2027-12-31
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 500907849
Hyphenated Format 50090-7849

Supplemental Identifiers

RxCUI
200033
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
  • 60 TABLET, FILM COATED in 1 BOTTLE (50090-7849-0)
  • 180 TABLET, FILM COATED in 1 BOTTLE (50090-7849-1)
  • 90 TABLET, FILM COATED in 1 BOTTLE (50090-7849-3)
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-7849-4)
source: ndc

Packages (4)

50090-7849-0 60 TABLET, FILM COATED in 1 BOTTLE (50090-7849-0) 50090-7849-1 180 TABLET, FILM COATED in 1 BOTTLE (50090-7849-1) 50090-7849-3 90 TABLET, FILM COATED in 1 BOTTLE (50090-7849-3) 50090-7849-4 30 TABLET, FILM COATED in 1 BOTTLE (50090-7849-4)

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": "fd7346c4-4f59-48ad-a3fd-d64636e10952", "openfda": {"nui": ["N0000000099", "N0000009923", "N0000009924", "N0000175553", "N0000175556"], "unii": ["0K47UL67F2"], "rxcui": ["200033"], "spl_set_id": ["947baca7-f9c8-4821-b47b-53c45288613e"], "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": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-7849-0)", "package_ndc": "50090-7849-0", "marketing_start_date": "20260106"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (50090-7849-1)", "package_ndc": "50090-7849-1", "marketing_start_date": "20260106"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7849-3)", "package_ndc": "50090-7849-3", "marketing_start_date": "20260106"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-7849-4)", "package_ndc": "50090-7849-4", "marketing_start_date": "20260106"}], "brand_name": "CARVEDILOL", "product_id": "50090-7849_fd7346c4-4f59-48ad-a3fd-d64636e10952", "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": "50090-7849", "generic_name": "CARVEDILOL", "labeler_name": "A-S Medication Solutions", "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": "20271231"}