venlafaxine hydrochloride

Generic: venlafaxine hydrochloride

Labeler: chartwell rx, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine hydrochloride
Generic Name venlafaxine hydrochloride
Labeler chartwell rx, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 225 mg/1

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-531
Product ID 62135-531_45adb66f-add1-678a-e063-6394a90a1f26
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209193
Listing Expiration 2026-12-31
Marketing Start 2019-12-26

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 62135531
Hyphenated Format 62135-531

Supplemental Identifiers

RxCUI
808748
UPC
0362135531300
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 ANDA209193 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 225 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (62135-531-30)
source: ndc

Packages (1)

62135-531-30 30 TABLET in 1 BOTTLE (62135-531-30)

Ingredients (1)

venlafaxine hydrochloride (225 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": "45adb66f-add1-678a-e063-6394a90a1f26", "openfda": {"upc": ["0362135531300"], "unii": ["7D7RX5A8MO"], "rxcui": ["808748"], "spl_set_id": ["85ec2d3f-49e4-4ac5-bd4a-c227589dbf58"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (62135-531-30)", "package_ndc": "62135-531-30", "marketing_start_date": "20230329"}], "brand_name": "venlafaxine hydrochloride", "product_id": "62135-531_45adb66f-add1-678a-e063-6394a90a1f26", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "62135-531", "generic_name": "venlafaxine hydrochloride", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "225 mg/1"}], "application_number": "ANDA209193", "marketing_category": "ANDA", "marketing_start_date": "20191226", "listing_expiration_date": "20261231"}