desvenlafaxine
Generic: desvenlafaxine succinate
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
desvenlafaxine
Generic Name
desvenlafaxine succinate
Labeler
preferred pharmaceuticals inc.
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
desvenlafaxine succinate 100 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687887175
Hyphenated Format
68788-7175
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 100 mg/1
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)
Packages (4)
Ingredients (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"}