desvenlafaxine
Generic: desvenlafaxine
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
desvenlafaxine
Generic Name
desvenlafaxine
Labeler
bryant ranch prepack
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
desvenlafaxine succinate 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-1815
Product ID
71335-1815_a2058611-ab91-4b2f-928c-3efea6bf0006
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210014
Listing Expiration
2026-12-31
Marketing Start
2020-08-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713351815
Hyphenated Format
71335-1815
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 (source: ndc)
Application Number
ANDA210014 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-1815-1)
- 28 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-1815-2)
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-1815-3)
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-1815-4)
Packages (4)
71335-1815-1
30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-1815-1)
71335-1815-2
28 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-1815-2)
71335-1815-3
90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-1815-3)
71335-1815-4
60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-1815-4)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a2058611-ab91-4b2f-928c-3efea6bf0006", "openfda": {"unii": ["ZB22ENF0XR"], "rxcui": ["1874553"], "spl_set_id": ["6741bdef-dc58-47be-b28d-c43476dc8bde"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-1815-1)", "package_ndc": "71335-1815-1", "marketing_start_date": "20210319"}, {"sample": false, "description": "28 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-1815-2)", "package_ndc": "71335-1815-2", "marketing_start_date": "20240717"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-1815-3)", "package_ndc": "71335-1815-3", "marketing_start_date": "20240606"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-1815-4)", "package_ndc": "71335-1815-4", "marketing_start_date": "20240717"}], "brand_name": "Desvenlafaxine", "product_id": "71335-1815_a2058611-ab91-4b2f-928c-3efea6bf0006", "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": "71335-1815", "generic_name": "Desvenlafaxine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desvenlafaxine", "active_ingredients": [{"name": "DESVENLAFAXINE SUCCINATE", "strength": "100 mg/1"}], "application_number": "ANDA210014", "marketing_category": "ANDA", "marketing_start_date": "20200801", "listing_expiration_date": "20261231"}