desvenlafaxine

Generic: desvenlafaxine

Labeler: northstar rx llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name desvenlafaxine
Generic Name desvenlafaxine
Labeler northstar rx llc
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

desvenlafaxine succinate 100 mg/1

Manufacturer
NorthStar Rx LLC

Identifiers & Regulatory

Product NDC 72603-557
Product ID 72603-557_34888df6-f68d-c171-e063-6294a90a7604
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204028
Listing Expiration 2026-12-31
Marketing Start 2025-05-02

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 72603557
Hyphenated Format 72603-557

Supplemental Identifiers

RxCUI
1607617 1874553 1874559
UPC
0372603555011 0372603557015 0372603556025 0372603556018
UNII
ZB22ENF0XR

Packaging Origin

Original Packager
true

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 90 TABLET, EXTENDED RELEASE in 1 PACKAGE (72603-557-01)
source: ndc

Packages (1)

72603-557-01 90 TABLET, EXTENDED RELEASE in 1 PACKAGE (72603-557-01)

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": "34888df6-f68d-c171-e063-6294a90a7604", "openfda": {"upc": ["0372603555011", "0372603557015", "0372603556025", "0372603556018"], "unii": ["ZB22ENF0XR"], "rxcui": ["1607617", "1874553", "1874559"], "spl_set_id": ["3fcc0555-f9cf-4735-a0ef-830c50c390b8"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 PACKAGE (72603-557-01)", "package_ndc": "72603-557-01", "marketing_start_date": "20250502"}], "brand_name": "DESVENLAFAXINE", "product_id": "72603-557_34888df6-f68d-c171-e063-6294a90a7604", "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": "72603-557", "generic_name": "DESVENLAFAXINE", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DESVENLAFAXINE", "active_ingredients": [{"name": "DESVENLAFAXINE SUCCINATE", "strength": "100 mg/1"}], "application_number": "ANDA204028", "marketing_category": "ANDA", "marketing_start_date": "20250502", "listing_expiration_date": "20261231"}