desvenlafaxine

Generic: desvenlafaxine

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name desvenlafaxine
Generic Name desvenlafaxine
Labeler american health packaging
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

desvenlafaxine succinate 50 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-607
Product ID 60687-607_2423ba9f-e3f1-de11-e063-6294a90a64fd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204082
Listing Expiration 2026-12-31
Marketing Start 2021-12-01

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 60687607
Hyphenated Format 60687-607

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 ANDA204082 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-607-21) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-607-11)
source: ndc

Packages (1)

60687-607-21 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-607-21) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-607-11)

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": "2423ba9f-e3f1-de11-e063-6294a90a64fd", "openfda": {"unii": ["ZB22ENF0XR"], "rxcui": ["1874559"], "spl_set_id": ["e0dbbdbc-9438-407a-b3e1-f3bb7f177a4e"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-607-21)  / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-607-11)", "package_ndc": "60687-607-21", "marketing_start_date": "20211201"}], "brand_name": "Desvenlafaxine", "product_id": "60687-607_2423ba9f-e3f1-de11-e063-6294a90a64fd", "dosage_form": "TABLET, FILM COATED, 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": "60687-607", "generic_name": "Desvenlafaxine", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desvenlafaxine", "active_ingredients": [{"name": "DESVENLAFAXINE SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA204082", "marketing_category": "ANDA", "marketing_start_date": "20211201", "listing_expiration_date": "20261231"}