venlafaxine

Generic: venlafaxine

Labeler: almatica pharma llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine
Generic Name venlafaxine
Labeler almatica pharma llc
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

venlafaxine besylate monohydrate 112.5 mg/1

Manufacturer
Almatica Pharma LLC

Identifiers & Regulatory

Product NDC 52427-632
Product ID 52427-632_1b0762be-0db0-b997-b76b-b212a496f82c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA215429
Listing Expiration 2026-12-31
Marketing Start 2022-06-30

Pharmacologic Class

Classes
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 52427632
Hyphenated Format 52427-632

Supplemental Identifiers

RxCUI
2605950
UPC
0352427632303
UNII
18XP3YT5NH

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 venlafaxine (source: ndc)
Generic Name venlafaxine (source: ndc)
Application Number NDA215429 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 112.5 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (52427-632-30)
source: ndc

Packages (1)

52427-632-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (52427-632-30)

Ingredients (1)

venlafaxine besylate monohydrate (112.5 mg/1)

Linked Drug Pages (1)

venlafaxine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1b0762be-0db0-b997-b76b-b212a496f82c", "openfda": {"upc": ["0352427632303"], "unii": ["18XP3YT5NH"], "rxcui": ["2605950"], "spl_set_id": ["e81a2daf-b8b2-7c05-b532-bc775700b100"], "manufacturer_name": ["Almatica Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (52427-632-30)", "package_ndc": "52427-632-30", "marketing_start_date": "20220801"}], "brand_name": "venlafaxine", "product_id": "52427-632_1b0762be-0db0-b997-b76b-b212a496f82c", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "52427-632", "generic_name": "venlafaxine", "labeler_name": "Almatica Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE BESYLATE MONOHYDRATE", "strength": "112.5 mg/1"}], "application_number": "NDA215429", "marketing_category": "NDA", "marketing_start_date": "20220630", "listing_expiration_date": "20261231"}