desvenlafaxine succinate

Generic: desvenlafaxine succinate

Labeler: lupin pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name desvenlafaxine succinate
Generic Name desvenlafaxine succinate
Labeler lupin pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

desvenlafaxine succinate 100 mg/1

Manufacturer
Lupin Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68180-593
Product ID 68180-593_748a4941-405f-436f-933b-0bec4b119e3c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204172
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 68180593
Hyphenated Format 68180-593

Supplemental Identifiers

RxCUI
1607617 1874553 1874559
UPC
0368180593065 0368180592068 0368180604068
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 succinate (source: ndc)
Generic Name desvenlafaxine succinate (source: ndc)
Application Number ANDA204172 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68180-593-06)
source: ndc

Packages (1)

68180-593-06 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68180-593-06)

Ingredients (1)

desvenlafaxine succinate (100 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": "748a4941-405f-436f-933b-0bec4b119e3c", "openfda": {"upc": ["0368180593065", "0368180592068", "0368180604068"], "unii": ["ZB22ENF0XR"], "rxcui": ["1607617", "1874553", "1874559"], "spl_set_id": ["e96272a2-8f73-4fbe-a8d4-a78d4ad68831"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68180-593-06)", "package_ndc": "68180-593-06", "marketing_start_date": "20170301"}], "brand_name": "Desvenlafaxine Succinate", "product_id": "68180-593_748a4941-405f-436f-933b-0bec4b119e3c", "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": "68180-593", "generic_name": "Desvenlafaxine Succinate", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desvenlafaxine Succinate", "active_ingredients": [{"name": "DESVENLAFAXINE SUCCINATE", "strength": "100 mg/1"}], "application_number": "ANDA204172", "marketing_category": "ANDA", "marketing_start_date": "20170301", "listing_expiration_date": "20261231"}