carvedilol
Generic: carvedilol
Labeler: qpharma incDrug Facts
Product Profile
Brand Name
carvedilol
Generic Name
carvedilol
Labeler
qpharma inc
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
carvedilol 3.125 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
42708-181
Product ID
42708-181_45871b50-d2fc-68c5-e063-6394a90aa1e8
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
42708181
Hyphenated Format
42708-181
Supplemental Identifiers
RxCUI
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
- 3.125 mg/1
Packaging
- 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-181-60)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45871b50-d2fc-68c5-e063-6394a90aa1e8", "openfda": {"nui": ["N0000000099", "N0000009923", "N0000009924", "N0000175553", "N0000175556"], "unii": ["0K47UL67F2"], "rxcui": ["686924"], "spl_set_id": ["010290af-81f4-0037-e063-6394a90a4638"], "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": ["QPharma Inc"]}, "finished": true, "packaging": [{"sample": true, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-181-60)", "package_ndc": "42708-181-60", "marketing_start_date": "20230804"}], "brand_name": "Carvedilol", "product_id": "42708-181_45871b50-d2fc-68c5-e063-6394a90aa1e8", "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": "42708-181", "generic_name": "Carvedilol", "labeler_name": "QPharma Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Carvedilol", "active_ingredients": [{"name": "CARVEDILOL", "strength": "3.125 mg/1"}], "application_number": "ANDA077614", "marketing_category": "ANDA", "marketing_start_date": "20070905", "listing_expiration_date": "20261231"}