desvenlafaxine
Generic: desvenlafaxine
Labeler: advagen pharma ltdDrug Facts
Product Profile
Brand Name
desvenlafaxine
Generic Name
desvenlafaxine
Labeler
advagen pharma ltd
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
desvenlafaxine succinate 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72888-143
Product ID
72888-143_4859d9c4-bb8c-477b-e063-6294a90a7cb9
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204028
Listing Expiration
2027-12-31
Marketing Start
2022-01-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72888143
Hyphenated Format
72888-143
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
desvenlafaxine (source: ndc)
Generic Name
desvenlafaxine (source: ndc)
Application Number
ANDA204028 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 1000 TABLET, EXTENDED RELEASE in 1 PACKAGE (72888-143-00)
- 500 TABLET, EXTENDED RELEASE in 1 PACKAGE (72888-143-05)
- 30 TABLET, EXTENDED RELEASE in 1 PACKAGE (72888-143-30)
- 90 TABLET, EXTENDED RELEASE in 1 PACKAGE (72888-143-90)
Packages (4)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4859d9c4-bb8c-477b-e063-6294a90a7cb9", "openfda": {"upc": ["0372888175003", "0372888175058", "0372888144054", "0372888144900", "0372888144009", "0372888143903", "0372888143309", "0372888143002", "0372888175904", "0372888143057", "0372888144306"], "unii": ["ZB22ENF0XR"], "rxcui": ["1607617", "1874553", "1874559"], "spl_set_id": ["ff837eb1-24c3-4c63-9b4b-c6b5935a9b47"], "manufacturer_name": ["Advagen Pharma Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 PACKAGE (72888-143-00)", "package_ndc": "72888-143-00", "marketing_start_date": "20220131"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 PACKAGE (72888-143-05)", "package_ndc": "72888-143-05", "marketing_start_date": "20220131"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 PACKAGE (72888-143-30)", "package_ndc": "72888-143-30", "marketing_start_date": "20220131"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 PACKAGE (72888-143-90)", "package_ndc": "72888-143-90", "marketing_start_date": "20220131"}], "brand_name": "DESVENLAFAXINE", "product_id": "72888-143_4859d9c4-bb8c-477b-e063-6294a90a7cb9", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "72888-143", "generic_name": "DESVENLAFAXINE", "labeler_name": "Advagen Pharma Ltd", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DESVENLAFAXINE", "active_ingredients": [{"name": "DESVENLAFAXINE SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA204028", "marketing_category": "ANDA", "marketing_start_date": "20220131", "listing_expiration_date": "20271231"}