desvenlafaxine
Generic: desvenlafaxine succinate
Labeler: direct rxDrug Facts
Product Profile
Brand Name
desvenlafaxine
Generic Name
desvenlafaxine succinate
Labeler
direct rx
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
desvenlafaxine succinate 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72189-147
Product ID
72189-147_2be9051e-2257-8882-e063-6294a90a543a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204003
Listing Expiration
2026-12-31
Marketing Start
2020-11-12
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72189147
Hyphenated Format
72189-147
Supplemental Identifiers
RxCUI
UNII
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 succinate (source: ndc)
Application Number
ANDA204003 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 28 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-147-28)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2be9051e-2257-8882-e063-6294a90a543a", "openfda": {"unii": ["ZB22ENF0XR"], "rxcui": ["1874559"], "spl_set_id": ["b3ef2bb2-c336-2d57-e053-2995a90a5fe0"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "28 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-147-28)", "package_ndc": "72189-147-28", "marketing_start_date": "20201112"}], "brand_name": "desvenlafaxine", "product_id": "72189-147_2be9051e-2257-8882-e063-6294a90a543a", "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": "72189-147", "generic_name": "desvenlafaxine succinate", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "desvenlafaxine", "active_ingredients": [{"name": "DESVENLAFAXINE SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA204003", "marketing_category": "ANDA", "marketing_start_date": "20201112", "listing_expiration_date": "20261231"}