invokamet xr
Generic: canagliflozin and metformin hydrochloride
Labeler: janssen pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
invokamet xr
Generic Name
canagliflozin and metformin hydrochloride
Labeler
janssen pharmaceuticals, inc.
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Routes
Active Ingredients
canagliflozin 150 mg/1, metformin hydrochloride 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50458-942
Product ID
50458-942_3ce5755e-f0a3-692b-e063-6294a90a3c1f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA205879
Listing Expiration
2026-12-31
Marketing Start
2016-09-20
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
50458942
Hyphenated Format
50458-942
Supplemental Identifiers
RxCUI
UPC
UNII
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
invokamet xr (source: ndc)
Generic Name
canagliflozin and metformin hydrochloride (source: ndc)
Application Number
NDA205879 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 150 mg/1
- 500 mg/1
Packaging
- 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50458-942-01)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3ce5755e-f0a3-692b-e063-6294a90a3c1f", "openfda": {"upc": ["0350458543605", "0350458541601"], "unii": ["0SAC974Z85", "786Z46389E"], "rxcui": ["1545150", "1545156", "1545157", "1545159", "1545161", "1545163", "1545164", "1545166", "1810997", "1810999", "1811002", "1811003", "1811006", "1811007", "1811010", "1811011"], "spl_set_id": ["6868666b-c25e-40d1-9d1f-306bbe9390c1"], "manufacturer_name": ["Janssen Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50458-942-01)", "package_ndc": "50458-942-01", "marketing_start_date": "20160920"}], "brand_name": "INVOKAMET XR", "product_id": "50458-942_3ce5755e-f0a3-692b-e063-6294a90a3c1f", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]", "P-Glycoprotein Inhibitors [MoA]", "Sodium-Glucose Cotransporter 2 Inhibitor [EPC]", "Sodium-Glucose Transporter 2 Inhibitors [MoA]"], "product_ndc": "50458-942", "generic_name": "canagliflozin and metformin hydrochloride", "labeler_name": "Janssen Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "INVOKAMET XR", "active_ingredients": [{"name": "CANAGLIFLOZIN", "strength": "150 mg/1"}, {"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "NDA205879", "marketing_category": "NDA", "marketing_start_date": "20160920", "listing_expiration_date": "20261231"}