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 100 mg/1

Manufacturer
Bryant Ranch Prepack

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
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 713351815
Hyphenated Format 71335-1815

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

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
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)
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": "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"}