desvenlafaxine er

Generic: desvenlafaxine er

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name desvenlafaxine er
Generic Name desvenlafaxine er
Labeler direct_rx
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

desvenlafaxine succinate 50 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 61919-882
Product ID 61919-882_4c49ea72-e09e-fa7c-e063-6294a90aba89
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204172
Listing Expiration 2027-12-31
Marketing Start 2019-06-04

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 61919882
Hyphenated Format 61919-882

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 er (source: ndc)
Generic Name desvenlafaxine er (source: ndc)
Application Number ANDA204172 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (61919-882-28)
  • 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (61919-882-30)
  • 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (61919-882-60)
source: ndc

Packages (3)

61919-882-28 28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (61919-882-28) 61919-882-30 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (61919-882-30) 61919-882-60 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (61919-882-60)

Ingredients (1)

desvenlafaxine succinate (50 mg/1)

Linked Drug Pages (1)

DESVENLAFAXINE ER ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4c49ea72-e09e-fa7c-e063-6294a90aba89", "openfda": {"unii": ["ZB22ENF0XR"], "rxcui": ["1874559"], "spl_set_id": ["8a834c66-846e-38a8-e053-2a95a90a4035"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (61919-882-28)", "package_ndc": "61919-882-28", "marketing_start_date": "20190604"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (61919-882-30)", "package_ndc": "61919-882-30", "marketing_start_date": "20190604"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (61919-882-60)", "package_ndc": "61919-882-60", "marketing_start_date": "20190604"}], "brand_name": "DESVENLAFAXINE ER", "product_id": "61919-882_4c49ea72-e09e-fa7c-e063-6294a90aba89", "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": "61919-882", "generic_name": "DESVENLAFAXINE ER", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DESVENLAFAXINE ER", "active_ingredients": [{"name": "DESVENLAFAXINE SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA204172", "marketing_category": "ANDA", "marketing_start_date": "20190604", "listing_expiration_date": "20271231"}