desvenlafaxine

Generic: desvenlafaxine

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name desvenlafaxine
Generic Name desvenlafaxine
Labeler nucare pharmaceuticals,inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

desvenlafaxine succinate 50 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-3790
Product ID 68071-3790_2e5bc1dd-0f1d-7f11-e063-6394a90ad3a2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204028
Listing Expiration 2026-12-31
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 680713790
Hyphenated Format 68071-3790

Supplemental Identifiers

RxCUI
1874559
UPC
0368071379037
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 ANDA204028 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-3790-3)
source: ndc

Packages (1)

68071-3790-3 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-3790-3)

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": "2e5bc1dd-0f1d-7f11-e063-6394a90ad3a2", "openfda": {"upc": ["0368071379037"], "unii": ["ZB22ENF0XR"], "rxcui": ["1874559"], "spl_set_id": ["2dce1542-ead5-1b24-e063-6294a90a6df0"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-3790-3)", "package_ndc": "68071-3790-3", "marketing_start_date": "20250210"}], "brand_name": "DESVENLAFAXINE", "product_id": "68071-3790_2e5bc1dd-0f1d-7f11-e063-6394a90ad3a2", "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": "68071-3790", "generic_name": "DESVENLAFAXINE", "labeler_name": "NuCare Pharmaceuticals,Inc.", "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": "20261231"}