venlafaxine hydrochloride

Generic: venlafaxine hydrochloride

Labeler: avpak
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine hydrochloride
Generic Name venlafaxine hydrochloride
Labeler avpak
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 150 mg/1

Manufacturer
AvPAK

Identifiers & Regulatory

Product NDC 50268-875
Product ID 50268-875_2efde399-c009-de89-e063-6394a90a7e0f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212277
Listing Expiration 2026-12-31
Marketing Start 2025-02-25

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 50268875
Hyphenated Format 50268-875

Supplemental Identifiers

RxCUI
313581 313583 313585
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 hydrochloride (source: ndc)
Generic Name venlafaxine hydrochloride (source: ndc)
Application Number ANDA212277 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 50 BLISTER PACK in 1 BOX (50268-875-15) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (50268-875-11)
source: ndc

Packages (1)

50268-875-15 50 BLISTER PACK in 1 BOX (50268-875-15) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (50268-875-11)

Ingredients (1)

venlafaxine hydrochloride (150 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": "2efde399-c009-de89-e063-6394a90a7e0f", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313581", "313583", "313585"], "spl_set_id": ["2efde38c-250e-d1b9-e063-6394a90a1b74"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-875-15)  / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (50268-875-11)", "package_ndc": "50268-875-15", "marketing_start_date": "20250225"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "50268-875_2efde399-c009-de89-e063-6394a90a7e0f", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "50268-875", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA212277", "marketing_category": "ANDA", "marketing_start_date": "20250225", "listing_expiration_date": "20261231"}