carvedilol
Generic: carvedilol
Labeler: qpharma, inc.Drug 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
42708-072
Product ID
42708-072_45b3b81e-d875-5d61-e063-6394a90ad20a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076373
Listing Expiration
2026-12-31
Marketing Start
2007-09-06
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
42708072
Hyphenated Format
42708-072
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
ANDA076373 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 3.125 mg/1
Packaging
- 60 TABLET, FILM COATED in 1 BOTTLE (42708-072-60)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45b3b81e-d875-5d61-e063-6394a90ad20a", "openfda": {"nui": ["N0000000099", "N0000009923", "N0000009924", "N0000175553", "N0000175556"], "unii": ["0K47UL67F2"], "rxcui": ["686924"], "spl_set_id": ["ffbedcce-0d64-4aed-9e65-09448d71ca91"], "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 (42708-072-60)", "package_ndc": "42708-072-60", "marketing_start_date": "20180418"}], "brand_name": "Carvedilol", "product_id": "42708-072_45b3b81e-d875-5d61-e063-6394a90ad20a", "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": "42708-072", "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": "ANDA076373", "marketing_category": "ANDA", "marketing_start_date": "20070906", "listing_expiration_date": "20261231"}