venlafaxine

Generic: venlafaxine

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine
Generic Name venlafaxine
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 100 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-752
Product ID 63187-752_0a1e4108-e2a9-4c22-ab48-900d3bc20c1d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078932
Listing Expiration 2026-12-31
Marketing Start 2015-10-01

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 63187752
Hyphenated Format 63187-752

Supplemental Identifiers

RxCUI
313580
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 (source: ndc)
Application Number ANDA078932 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (63187-752-30)
  • 60 TABLET in 1 BOTTLE (63187-752-60)
  • 90 TABLET in 1 BOTTLE (63187-752-90)
source: ndc

Packages (3)

63187-752-30 30 TABLET in 1 BOTTLE (63187-752-30) 63187-752-60 60 TABLET in 1 BOTTLE (63187-752-60) 63187-752-90 90 TABLET in 1 BOTTLE (63187-752-90)

Ingredients (1)

venlafaxine hydrochloride (100 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": "0a1e4108-e2a9-4c22-ab48-900d3bc20c1d", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313580"], "spl_set_id": ["cc3a1258-aafb-48cf-86f7-fcf59e0c6cdd"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (63187-752-30)", "package_ndc": "63187-752-30", "marketing_start_date": "20161003"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63187-752-60)", "package_ndc": "63187-752-60", "marketing_start_date": "20161003"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (63187-752-90)", "package_ndc": "63187-752-90", "marketing_start_date": "20161003"}], "brand_name": "venlafaxine", "product_id": "63187-752_0a1e4108-e2a9-4c22-ab48-900d3bc20c1d", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "63187-752", "generic_name": "venlafaxine", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA078932", "marketing_category": "ANDA", "marketing_start_date": "20151001", "listing_expiration_date": "20261231"}