desvenlafaxine

Generic: desvenlafaxine succinate

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name desvenlafaxine
Generic Name desvenlafaxine succinate
Labeler proficient rx lp
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

desvenlafaxine succinate 100 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-586
Product ID 71205-586_39cdc974-0387-41dd-946b-4f8b77066ff5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204003
Listing Expiration 2026-12-31
Marketing Start 2017-03-01

Pharmacologic Class

Classes
cytochrome p450 2d6 inhibitors [moa] norepinephrine uptake inhibitors [moa] serotonin uptake inhibitors [moa] serotonin and norepinephrine reuptake inhibitor [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205586
Hyphenated Format 71205-586

Supplemental Identifiers

RxCUI
1874553
UPC
0371205586300
UNII
ZB22ENF0XR

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-586-30)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-586-60)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-586-90)
source: ndc

Packages (3)

71205-586-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-586-30) 71205-586-60 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-586-60) 71205-586-90 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-586-90)

Ingredients (1)

desvenlafaxine succinate (100 mg/1)

Linked Drug Pages (1)

Desvenlafaxine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "39cdc974-0387-41dd-946b-4f8b77066ff5", "openfda": {"upc": ["0371205586300"], "unii": ["ZB22ENF0XR"], "rxcui": ["1874553"], "spl_set_id": ["d4542c5e-f9e8-49c7-afa6-9dd4c4d485f2"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-586-30)", "package_ndc": "71205-586-30", "marketing_start_date": "20210707"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-586-60)", "package_ndc": "71205-586-60", "marketing_start_date": "20210707"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-586-90)", "package_ndc": "71205-586-90", "marketing_start_date": "20210707"}], "brand_name": "Desvenlafaxine", "product_id": "71205-586_39cdc974-0387-41dd-946b-4f8b77066ff5", "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": "71205-586", "generic_name": "Desvenlafaxine Succinate", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desvenlafaxine", "active_ingredients": [{"name": "DESVENLAFAXINE SUCCINATE", "strength": "100 mg/1"}], "application_number": "ANDA204003", "marketing_category": "ANDA", "marketing_start_date": "20170301", "listing_expiration_date": "20261231"}