desvenlafaxine er

Generic: desvenlafaxine er

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name desvenlafaxine er
Generic Name desvenlafaxine er
Labeler direct_rx
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

desvenlafaxine succinate 50 mg/1

Manufacturer
Direct_rx

Identifiers & Regulatory

Product NDC 72189-567
Product ID 72189-567_34f5586c-4441-54fb-e063-6394a90aa90d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204028
Listing Expiration 2026-12-31
Marketing Start 2024-07-18

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 72189567
Hyphenated Format 72189-567

Supplemental Identifiers

RxCUI
1874559
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 er (source: ndc)
Generic Name desvenlafaxine er (source: ndc)
Application Number ANDA204028 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 28 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-567-28)
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-567-30)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-567-60)
source: ndc

Packages (3)

72189-567-28 28 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-567-28) 72189-567-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-567-30) 72189-567-60 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-567-60)

Ingredients (1)

desvenlafaxine succinate (50 mg/1)

Linked Drug Pages (1)

Desvenlafaxine ER ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "34f5586c-4441-54fb-e063-6394a90aa90d", "openfda": {"unii": ["ZB22ENF0XR"], "rxcui": ["1874559"], "spl_set_id": ["1d86d1dc-d685-43aa-e063-6294a90a9907"], "manufacturer_name": ["Direct_rx"]}, "finished": true, "packaging": [{"sample": false, "description": "28 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-567-28)", "package_ndc": "72189-567-28", "marketing_start_date": "20240718"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-567-30)", "package_ndc": "72189-567-30", "marketing_start_date": "20240718"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-567-60)", "package_ndc": "72189-567-60", "marketing_start_date": "20240718"}], "brand_name": "Desvenlafaxine ER", "product_id": "72189-567_34f5586c-4441-54fb-e063-6394a90aa90d", "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": "72189-567", "generic_name": "Desvenlafaxine ER", "labeler_name": "Direct_rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desvenlafaxine ER", "active_ingredients": [{"name": "DESVENLAFAXINE SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA204028", "marketing_category": "ANDA", "marketing_start_date": "20240718", "listing_expiration_date": "20261231"}