carvedilol
Generic: carvedilol
Labeler: nucare pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
carvedilol
Generic Name
carvedilol
Labeler
nucare pharmaceuticals,inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
carvedilol 12.5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68071-2230
Product ID
68071-2230_2ac0f53e-48b2-5d84-e063-6294a90a8ac8
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077614
Listing Expiration
2026-12-31
Marketing Start
2007-09-05
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680712230
Hyphenated Format
68071-2230
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
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
ANDA077614 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 12.5 mg/1
Packaging
- 180 TABLET, FILM COATED in 1 BOTTLE (68071-2230-3)
- 60 TABLET, FILM COATED in 1 BOTTLE (68071-2230-6)
- 180 TABLET, FILM COATED in 1 BOTTLE (68071-2230-8)
- 90 TABLET, FILM COATED in 1 BOTTLE (68071-2230-9)
Packages (4)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2ac0f53e-48b2-5d84-e063-6294a90a8ac8", "openfda": {"nui": ["N0000000099", "N0000009923", "N0000009924", "N0000175553", "N0000175556"], "upc": ["0368071223095"], "unii": ["0K47UL67F2"], "rxcui": ["200032"], "spl_set_id": ["ac14846e-423a-37c4-e053-2a95a90a3cdd"], "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": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (68071-2230-3)", "package_ndc": "68071-2230-3", "marketing_start_date": "20250102"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68071-2230-6)", "package_ndc": "68071-2230-6", "marketing_start_date": "20200804"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (68071-2230-8)", "package_ndc": "68071-2230-8", "marketing_start_date": "20200804"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68071-2230-9)", "package_ndc": "68071-2230-9", "marketing_start_date": "20200804"}], "brand_name": "Carvedilol", "product_id": "68071-2230_2ac0f53e-48b2-5d84-e063-6294a90a8ac8", "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": "68071-2230", "generic_name": "Carvedilol", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Carvedilol", "active_ingredients": [{"name": "CARVEDILOL", "strength": "12.5 mg/1"}], "application_number": "ANDA077614", "marketing_category": "ANDA", "marketing_start_date": "20070905", "listing_expiration_date": "20261231"}