desvenlafaxine

Generic: desvenlafaxine

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name desvenlafaxine
Generic Name desvenlafaxine
Labeler bryant ranch prepack
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

desvenlafaxine succinate 50 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1753
Product ID 71335-1753_d20af454-5f99-4a00-babd-b06c9c95a0f5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210014
Listing Expiration 2026-12-31
Marketing Start 2020-08-01

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 713351753
Hyphenated Format 71335-1753

Supplemental Identifiers

RxCUI
1874559
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 (source: ndc)
Application Number ANDA210014 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1753-1)
  • 28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1753-2)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1753-3)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1753-4)
  • 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1753-5)
source: ndc

Packages (5)

71335-1753-1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1753-1) 71335-1753-2 28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1753-2) 71335-1753-3 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1753-3) 71335-1753-4 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1753-4) 71335-1753-5 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1753-5)

Ingredients (1)

desvenlafaxine succinate (50 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": "d20af454-5f99-4a00-babd-b06c9c95a0f5", "openfda": {"unii": ["ZB22ENF0XR"], "rxcui": ["1874559"], "spl_set_id": ["a6c2316d-2a51-4975-a061-dc72f2724b2f"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1753-1)", "package_ndc": "71335-1753-1", "marketing_start_date": "20210112"}, {"sample": false, "description": "28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1753-2)", "package_ndc": "71335-1753-2", "marketing_start_date": "20240717"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1753-3)", "package_ndc": "71335-1753-3", "marketing_start_date": "20240717"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1753-4)", "package_ndc": "71335-1753-4", "marketing_start_date": "20210825"}, {"sample": false, "description": "180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1753-5)", "package_ndc": "71335-1753-5", "marketing_start_date": "20240717"}], "brand_name": "Desvenlafaxine", "product_id": "71335-1753_d20af454-5f99-4a00-babd-b06c9c95a0f5", "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": "71335-1753", "generic_name": "Desvenlafaxine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desvenlafaxine", "active_ingredients": [{"name": "DESVENLAFAXINE SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA210014", "marketing_category": "ANDA", "marketing_start_date": "20200801", "listing_expiration_date": "20261231"}