desvenlafaxine

Generic: desvenlafaxine

Labeler: advagen pharma ltd
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name desvenlafaxine
Generic Name desvenlafaxine
Labeler advagen pharma ltd
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

desvenlafaxine succinate 50 mg/1

Manufacturer
Advagen Pharma Ltd

Identifiers & Regulatory

Product NDC 72888-143
Product ID 72888-143_4859d9c4-bb8c-477b-e063-6294a90a7cb9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204028
Listing Expiration 2027-12-31
Marketing Start 2022-01-31

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 72888143
Hyphenated Format 72888-143

Supplemental Identifiers

RxCUI
1607617 1874553 1874559
UPC
0372888175003 0372888175058 0372888144054 0372888144900 0372888144009 0372888143903 0372888143309 0372888143002 0372888175904 0372888143057 0372888144306
UNII
ZB22ENF0XR

Packaging Origin

Original Packager
true

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 ANDA204028 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 1000 TABLET, EXTENDED RELEASE in 1 PACKAGE (72888-143-00)
  • 500 TABLET, EXTENDED RELEASE in 1 PACKAGE (72888-143-05)
  • 30 TABLET, EXTENDED RELEASE in 1 PACKAGE (72888-143-30)
  • 90 TABLET, EXTENDED RELEASE in 1 PACKAGE (72888-143-90)
source: ndc

Packages (4)

Ingredients (1)

desvenlafaxine succinate (50 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4859d9c4-bb8c-477b-e063-6294a90a7cb9", "openfda": {"upc": ["0372888175003", "0372888175058", "0372888144054", "0372888144900", "0372888144009", "0372888143903", "0372888143309", "0372888143002", "0372888175904", "0372888143057", "0372888144306"], "unii": ["ZB22ENF0XR"], "rxcui": ["1607617", "1874553", "1874559"], "spl_set_id": ["ff837eb1-24c3-4c63-9b4b-c6b5935a9b47"], "manufacturer_name": ["Advagen Pharma Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 PACKAGE (72888-143-00)", "package_ndc": "72888-143-00", "marketing_start_date": "20220131"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 PACKAGE (72888-143-05)", "package_ndc": "72888-143-05", "marketing_start_date": "20220131"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 PACKAGE (72888-143-30)", "package_ndc": "72888-143-30", "marketing_start_date": "20220131"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 PACKAGE (72888-143-90)", "package_ndc": "72888-143-90", "marketing_start_date": "20220131"}], "brand_name": "DESVENLAFAXINE", "product_id": "72888-143_4859d9c4-bb8c-477b-e063-6294a90a7cb9", "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": "72888-143", "generic_name": "DESVENLAFAXINE", "labeler_name": "Advagen Pharma Ltd", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DESVENLAFAXINE", "active_ingredients": [{"name": "DESVENLAFAXINE SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA204028", "marketing_category": "ANDA", "marketing_start_date": "20220131", "listing_expiration_date": "20271231"}