venlafaxine hydrochloride

Generic: venlafaxine hydrochloride

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

Drug Facts

Product Profile

Brand Name venlafaxine hydrochloride
Generic Name venlafaxine hydrochloride
Labeler teva pharmaceuticals usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 37.5 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-9148
Product ID 0093-9148_da23a2ab-f20e-4208-b72b-d50260b97923
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076690
Listing Expiration 2026-12-31
Marketing Start 2006-08-04

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 00939148
Hyphenated Format 0093-9148

Supplemental Identifiers

RxCUI
313580 313582 313584 313586 314277
UPC
0300939148010 0300939149017 0300939163013 0300939147013 0300939157012
UNII
7D7RX5A8MO

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 hydrochloride (source: ndc)
Generic Name venlafaxine hydrochloride (source: ndc)
Application Number ANDA076690 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 37.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (0093-9148-01)
source: ndc

Packages (1)

0093-9148-01 100 TABLET in 1 BOTTLE (0093-9148-01)

Ingredients (1)

venlafaxine hydrochloride (37.5 mg/1)

Linked Drug Pages (1)

Venlafaxine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "da23a2ab-f20e-4208-b72b-d50260b97923", "openfda": {"upc": ["0300939148010", "0300939149017", "0300939163013", "0300939147013", "0300939157012"], "unii": ["7D7RX5A8MO"], "rxcui": ["313580", "313582", "313584", "313586", "314277"], "spl_set_id": ["37aaa8ac-4e0c-4e04-98b5-19b0d90d857c"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0093-9148-01)", "package_ndc": "0093-9148-01", "marketing_start_date": "20060804"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "0093-9148_da23a2ab-f20e-4208-b72b-d50260b97923", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "0093-9148", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA076690", "marketing_category": "ANDA", "marketing_start_date": "20060804", "listing_expiration_date": "20261231"}