desvenlafaxine

Generic: desvenlafaxine

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name desvenlafaxine
Generic Name desvenlafaxine
Labeler sun pharmaceutical industries, inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

desvenlafaxine 100 mg/1

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 63304-192
Product ID 63304-192_cd04a0b2-a7f2-4629-997f-af2a8e65f15b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA204150
Listing Expiration 2026-12-31
Marketing Start 2013-03-05

Pharmacologic Class

Established (EPC)
serotonin and norepinephrine reuptake inhibitor [epc]
Mechanism of Action
norepinephrine uptake inhibitors [moa] serotonin uptake inhibitors [moa] cytochrome p450 2d6 inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63304192
Hyphenated Format 63304-192

Supplemental Identifiers

RxCUI
790264 790288
UNII
NG99554ANW
NUI
N0000000102 N0000175749 N0000000109 N0000182137

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 NDA204150 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-192-30)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-192-90)
source: ndc

Packages (2)

63304-192-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-192-30) 63304-192-90 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-192-90)

Ingredients (1)

desvenlafaxine (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": "cd04a0b2-a7f2-4629-997f-af2a8e65f15b", "openfda": {"nui": ["N0000000102", "N0000175749", "N0000000109", "N0000182137"], "unii": ["NG99554ANW"], "rxcui": ["790264", "790288"], "spl_set_id": ["91cf39c9-4d26-480a-a3a3-a3d8d4c4d222"], "pharm_class_epc": ["Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "pharm_class_moa": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Cytochrome P450 2D6 Inhibitors [MoA]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-192-30)", "package_ndc": "63304-192-30", "marketing_start_date": "20130305"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-192-90)", "package_ndc": "63304-192-90", "marketing_start_date": "20130305"}], "brand_name": "Desvenlafaxine", "product_id": "63304-192_cd04a0b2-a7f2-4629-997f-af2a8e65f15b", "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": "63304-192", "generic_name": "Desvenlafaxine", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desvenlafaxine", "active_ingredients": [{"name": "DESVENLAFAXINE", "strength": "100 mg/1"}], "application_number": "NDA204150", "marketing_category": "NDA", "marketing_start_date": "20130305", "listing_expiration_date": "20261231"}