venlafaxine hydrochloride

Generic: venlafaxine hydrochloride

Labeler: advagen pharma ltd.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine hydrochloride
Generic Name venlafaxine hydrochloride
Labeler advagen pharma ltd.
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 37.5 mg/1

Manufacturer
Advagen Pharma Ltd.

Identifiers & Regulatory

Product NDC 72888-179
Product ID 72888-179_28d7b772-877d-511e-e063-6294a90ab3fd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203332
Listing Expiration 2026-12-31
Marketing Start 2020-03-20

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 72888179
Hyphenated Format 72888-179

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 ANDA203332 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 37.5 mg/1
source: ndc
Packaging
  • 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72888-179-30)
  • 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72888-179-90)
source: ndc

Packages (2)

72888-179-30 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72888-179-30) 72888-179-90 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72888-179-90)

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": "28d7b772-877d-511e-e063-6294a90ab3fd", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313581", "313583", "313585"], "spl_set_id": ["48a75840-64e4-4d44-9a62-009373003105"], "manufacturer_name": ["Advagen Pharma Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72888-179-30)", "package_ndc": "72888-179-30", "marketing_start_date": "20200320"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72888-179-90)", "package_ndc": "72888-179-90", "marketing_start_date": "20200320"}], "brand_name": "VENLAFAXINE HYDROCHLORIDE", "product_id": "72888-179_28d7b772-877d-511e-e063-6294a90ab3fd", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "72888-179", "generic_name": "VENLAFAXINE HYDROCHLORIDE", "labeler_name": "Advagen Pharma Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VENLAFAXINE HYDROCHLORIDE", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA203332", "marketing_category": "ANDA", "marketing_start_date": "20200320", "listing_expiration_date": "20261231"}