venlafaxine

Generic: venlafaxine hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine
Generic Name venlafaxine hydrochloride
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 37.5 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-4853
Product ID 50090-4853_4858b2b3-fa81-4906-b002-5bb1d3bb100b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090555
Listing Expiration 2026-12-31
Marketing Start 2010-04-07

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 500904853
Hyphenated Format 50090-4853

Supplemental Identifiers

RxCUI
313584
UNII
7D7RX5A8MO

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 hydrochloride (source: ndc)
Application Number ANDA090555 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 37.5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-4853-0)
  • 90 TABLET in 1 BOTTLE (50090-4853-1)
source: ndc

Packages (2)

50090-4853-0 30 TABLET in 1 BOTTLE (50090-4853-0) 50090-4853-1 90 TABLET in 1 BOTTLE (50090-4853-1)

Ingredients (1)

venlafaxine hydrochloride (37.5 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": "4858b2b3-fa81-4906-b002-5bb1d3bb100b", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313584"], "spl_set_id": ["5bd03cf1-e8fc-44f3-9c41-06515b897f3b"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-4853-0)", "package_ndc": "50090-4853-0", "marketing_start_date": "20200120"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-4853-1)", "package_ndc": "50090-4853-1", "marketing_start_date": "20200120"}], "brand_name": "venlafaxine", "product_id": "50090-4853_4858b2b3-fa81-4906-b002-5bb1d3bb100b", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "50090-4853", "generic_name": "venlafaxine hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA090555", "marketing_category": "ANDA", "marketing_start_date": "20100407", "listing_expiration_date": "20261231"}