desvenlafaxine
Generic: desvenlafaxine succinate
Labeler: breckenridge pharmaceutical, incDrug Facts
Product Profile
Brand Name
desvenlafaxine
Generic Name
desvenlafaxine succinate
Labeler
breckenridge pharmaceutical, inc
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
desvenlafaxine succinate 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
51991-312
Product ID
51991-312_34b890a1-3d88-43fb-b54b-f168ae22ebc7
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204003
Listing Expiration
2026-12-31
Marketing Start
2017-03-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51991312
Hyphenated Format
51991-312
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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 succinate (source: ndc)
Application Number
ANDA204003 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (51991-312-01)
- 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (51991-312-10)
- 100 TABLET, EXTENDED RELEASE in 1 CARTON (51991-312-11)
- 14 TABLET, EXTENDED RELEASE in 1 BOTTLE (51991-312-14)
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (51991-312-33)
- 80 TABLET, EXTENDED RELEASE in 1 CARTON (51991-312-80)
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (51991-312-90)
Packages (7)
51991-312-01
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (51991-312-01)
51991-312-10
1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (51991-312-10)
51991-312-11
100 TABLET, EXTENDED RELEASE in 1 CARTON (51991-312-11)
51991-312-14
14 TABLET, EXTENDED RELEASE in 1 BOTTLE (51991-312-14)
51991-312-33
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (51991-312-33)
51991-312-80
80 TABLET, EXTENDED RELEASE in 1 CARTON (51991-312-80)
51991-312-90
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (51991-312-90)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "34b890a1-3d88-43fb-b54b-f168ae22ebc7", "openfda": {"upc": ["0351991006336"], "unii": ["ZB22ENF0XR"], "rxcui": ["1607617", "1874553", "1874559"], "spl_set_id": ["25bdfc41-c7cb-4d16-b6a8-f102f9b8c984"], "manufacturer_name": ["Breckenridge Pharmaceutical, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (51991-312-01)", "package_ndc": "51991-312-01", "marketing_start_date": "20170301"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (51991-312-10)", "package_ndc": "51991-312-10", "marketing_start_date": "20170301"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 CARTON (51991-312-11)", "package_ndc": "51991-312-11", "marketing_start_date": "20170301"}, {"sample": false, "description": "14 TABLET, EXTENDED RELEASE in 1 BOTTLE (51991-312-14)", "package_ndc": "51991-312-14", "marketing_start_date": "20170301"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (51991-312-33)", "package_ndc": "51991-312-33", "marketing_start_date": "20170301"}, {"sample": false, "description": "80 TABLET, EXTENDED RELEASE in 1 CARTON (51991-312-80)", "package_ndc": "51991-312-80", "marketing_start_date": "20170301"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (51991-312-90)", "package_ndc": "51991-312-90", "marketing_start_date": "20170301"}], "brand_name": "Desvenlafaxine", "product_id": "51991-312_34b890a1-3d88-43fb-b54b-f168ae22ebc7", "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": "51991-312", "generic_name": "Desvenlafaxine Succinate", "labeler_name": "Breckenridge Pharmaceutical, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desvenlafaxine", "active_ingredients": [{"name": "DESVENLAFAXINE SUCCINATE", "strength": "100 mg/1"}], "application_number": "ANDA204003", "marketing_category": "ANDA", "marketing_start_date": "20170301", "listing_expiration_date": "20261231"}