desvenlafaxine

Generic: desvenlafaxine succinate

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

Drug Facts

Product Profile

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

desvenlafaxine succinate 100 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-7175
Product ID 68788-7175_1f47a6d2-fc54-4fb6-ba94-74de796a55d9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204003
Listing Expiration 2026-12-31
Marketing Start 2018-06-11

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 687887175
Hyphenated Format 68788-7175

Supplemental Identifiers

RxCUI
1874553
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 (source: ndc)
Generic Name desvenlafaxine succinate (source: ndc)
Application Number ANDA204003 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7175-1)
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7175-3)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7175-6)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7175-9)
source: ndc

Packages (4)

Ingredients (1)

desvenlafaxine succinate (100 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1f47a6d2-fc54-4fb6-ba94-74de796a55d9", "openfda": {"unii": ["ZB22ENF0XR"], "rxcui": ["1874553"], "spl_set_id": ["b4a5efab-3765-4ea5-a8cd-66e67e76c845"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7175-1)", "package_ndc": "68788-7175-1", "marketing_start_date": "20180611"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7175-3)", "package_ndc": "68788-7175-3", "marketing_start_date": "20180611"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7175-6)", "package_ndc": "68788-7175-6", "marketing_start_date": "20180611"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7175-9)", "package_ndc": "68788-7175-9", "marketing_start_date": "20180611"}], "brand_name": "Desvenlafaxine", "product_id": "68788-7175_1f47a6d2-fc54-4fb6-ba94-74de796a55d9", "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": "68788-7175", "generic_name": "Desvenlafaxine Succinate", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desvenlafaxine", "active_ingredients": [{"name": "DESVENLAFAXINE SUCCINATE", "strength": "100 mg/1"}], "application_number": "ANDA204003", "marketing_category": "ANDA", "marketing_start_date": "20180611", "listing_expiration_date": "20261231"}