carvedilol
Generic: carvedilol
Labeler: glenmark pharmaceuticals inc., usaDrug Facts
Product Profile
Brand Name
carvedilol
Generic Name
carvedilol
Labeler
glenmark pharmaceuticals inc., usa
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
carvedilol 3.125 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68462-162
Product ID
68462-162_5f5b2d20-cc2a-4e91-b2b9-260e7438ab2c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078251
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
68462162
Hyphenated Format
68462-162
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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
ANDA078251 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 3.125 mg/1
Packaging
- 100 TABLET, FILM COATED in 1 BOTTLE (68462-162-01)
- 500 TABLET, FILM COATED in 1 BOTTLE (68462-162-05)
- 1000 TABLET, FILM COATED in 1 BOTTLE (68462-162-10)
- 180 TABLET, FILM COATED in 1 BOTTLE (68462-162-18)
- 60 TABLET, FILM COATED in 1 BOTTLE (68462-162-60)
Packages (5)
68462-162-01
100 TABLET, FILM COATED in 1 BOTTLE (68462-162-01)
68462-162-05
500 TABLET, FILM COATED in 1 BOTTLE (68462-162-05)
68462-162-10
1000 TABLET, FILM COATED in 1 BOTTLE (68462-162-10)
68462-162-18
180 TABLET, FILM COATED in 1 BOTTLE (68462-162-18)
68462-162-60
60 TABLET, FILM COATED in 1 BOTTLE (68462-162-60)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5f5b2d20-cc2a-4e91-b2b9-260e7438ab2c", "openfda": {"nui": ["N0000000099", "N0000009923", "N0000009924", "N0000175553", "N0000175556"], "upc": ["0368462162019", "0368462163016", "0368462164013", "0368462165010"], "unii": ["0K47UL67F2"], "rxcui": ["200031", "200032", "200033", "686924"], "spl_set_id": ["c4a21f67-7812-4634-beba-f8e85c63c5f2"], "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": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68462-162-01)", "package_ndc": "68462-162-01", "marketing_start_date": "20070905"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (68462-162-05)", "package_ndc": "68462-162-05", "marketing_start_date": "20070905"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (68462-162-10)", "package_ndc": "68462-162-10", "marketing_start_date": "20070905"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (68462-162-18)", "package_ndc": "68462-162-18", "marketing_start_date": "20141210"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68462-162-60)", "package_ndc": "68462-162-60", "marketing_start_date": "20070905"}], "brand_name": "Carvedilol", "product_id": "68462-162_5f5b2d20-cc2a-4e91-b2b9-260e7438ab2c", "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": "68462-162", "generic_name": "Carvedilol", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Carvedilol", "active_ingredients": [{"name": "CARVEDILOL", "strength": "3.125 mg/1"}], "application_number": "ANDA078251", "marketing_category": "ANDA", "marketing_start_date": "20070905", "listing_expiration_date": "20261231"}