venlafaxine hydrochloride

Generic: venlafaxine hydrochloride

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

Drug Facts

Product Profile

Brand Name venlafaxine hydrochloride
Generic Name venlafaxine hydrochloride
Labeler marlex pharmaceuticals, inc.
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 75 mg/1

Manufacturer
Marlex Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 10135-826
Product ID 10135-826_3d59e057-318b-f098-e063-6394a90a25be
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA201272
Listing Expiration 2026-12-31
Marketing Start 2025-08-01

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 10135826
Hyphenated Format 10135-826

Supplemental Identifiers

RxCUI
313581 313583 313585
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 ANDA201272 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (10135-826-10)
  • 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (10135-826-30)
  • 15 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (10135-826-75)
  • 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (10135-826-90)
source: ndc

Packages (4)

10135-826-10 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (10135-826-10) 10135-826-30 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (10135-826-30) 10135-826-75 15 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (10135-826-75) 10135-826-90 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (10135-826-90)

Ingredients (1)

venlafaxine hydrochloride (75 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": "3d59e057-318b-f098-e063-6394a90a25be", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313581", "313583", "313585"], "spl_set_id": ["3c2e188f-76aa-a022-e063-6294a90abfc9"], "manufacturer_name": ["Marlex Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (10135-826-10)", "package_ndc": "10135-826-10", "marketing_start_date": "20250801"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (10135-826-30)", "package_ndc": "10135-826-30", "marketing_start_date": "20250801"}, {"sample": false, "description": "15 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (10135-826-75)", "package_ndc": "10135-826-75", "marketing_start_date": "20250801"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (10135-826-90)", "package_ndc": "10135-826-90", "marketing_start_date": "20250801"}], "brand_name": "VENLAFAXINE HYDROCHLORIDE", "product_id": "10135-826_3d59e057-318b-f098-e063-6394a90a25be", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "10135-826", "generic_name": "VENLAFAXINE HYDROCHLORIDE", "labeler_name": "Marlex Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VENLAFAXINE HYDROCHLORIDE", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA201272", "marketing_category": "ANDA", "marketing_start_date": "20250801", "listing_expiration_date": "20261231"}