desvenlafaxine succinate

Generic: desvenlafaxine succinate

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name desvenlafaxine succinate
Generic Name desvenlafaxine succinate
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

desvenlafaxine succinate 25 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7468
Product ID 50090-7468_eb3e20e5-d136-463c-80ab-3d8fc16e0171
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204172
Listing Expiration 2026-12-31
Marketing Start 2022-08-25

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 500907468
Hyphenated Format 50090-7468

Supplemental Identifiers

RxCUI
1607617
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 succinate (source: ndc)
Generic Name desvenlafaxine succinate (source: ndc)
Application Number ANDA204172 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7468-0)
  • 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7468-1)
source: ndc

Packages (2)

50090-7468-0 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7468-0) 50090-7468-1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7468-1)

Ingredients (1)

desvenlafaxine succinate (25 mg/1)

Linked Drug Pages (1)

Desvenlafaxine Succinate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "eb3e20e5-d136-463c-80ab-3d8fc16e0171", "openfda": {"unii": ["ZB22ENF0XR"], "rxcui": ["1607617"], "spl_set_id": ["7ee04e8c-ce6c-450d-9122-2bffd170bfd7"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7468-0)", "package_ndc": "50090-7468-0", "marketing_start_date": "20241203"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7468-1)", "package_ndc": "50090-7468-1", "marketing_start_date": "20241203"}], "brand_name": "Desvenlafaxine Succinate", "product_id": "50090-7468_eb3e20e5-d136-463c-80ab-3d8fc16e0171", "dosage_form": "TABLET, FILM COATED, 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": "50090-7468", "generic_name": "Desvenlafaxine Succinate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desvenlafaxine Succinate", "active_ingredients": [{"name": "DESVENLAFAXINE SUCCINATE", "strength": "25 mg/1"}], "application_number": "ANDA204172", "marketing_category": "ANDA", "marketing_start_date": "20220825", "listing_expiration_date": "20261231"}