desvenlafaxine succinate
Generic: desvenlafaxine succinate
Labeler: macleods pharmaceuticals limitedDrug Facts
Product Profile
Brand Name
desvenlafaxine succinate
Generic Name
desvenlafaxine succinate
Labeler
macleods pharmaceuticals limited
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
desvenlafaxine succinate 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
33342-389
Product ID
33342-389_edf18b33-a226-44f8-9f42-c409e691ee64
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA211427
Listing Expiration
2026-12-31
Marketing Start
2018-06-16
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
33342389
Hyphenated Format
33342-389
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 succinate (source: ndc)
Generic Name
desvenlafaxine succinate (source: ndc)
Application Number
ANDA211427 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-389-07)
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-389-10)
- 10 BLISTER PACK in 1 CARTON (33342-389-12) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "edf18b33-a226-44f8-9f42-c409e691ee64", "openfda": {"upc": ["0333342389121", "0333342388100", "0333342389107", "0333342388070", "0333342388124", "0333342389077"], "unii": ["ZB22ENF0XR"], "rxcui": ["1874553", "1874559"], "spl_set_id": ["edf18b33-a226-44f8-9f42-c409e691ee64"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-389-07)", "package_ndc": "33342-389-07", "marketing_start_date": "20180616"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-389-10)", "package_ndc": "33342-389-10", "marketing_start_date": "20180616"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (33342-389-12) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "33342-389-12", "marketing_start_date": "20180616"}], "brand_name": "Desvenlafaxine Succinate", "product_id": "33342-389_edf18b33-a226-44f8-9f42-c409e691ee64", "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": "33342-389", "generic_name": "Desvenlafaxine Succinate", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desvenlafaxine Succinate", "active_ingredients": [{"name": "DESVENLAFAXINE SUCCINATE", "strength": "100 mg/1"}], "application_number": "ANDA211427", "marketing_category": "ANDA", "marketing_start_date": "20180616", "listing_expiration_date": "20261231"}