venlafaxine

Generic: venlafaxine

Labeler: ascend laboratories, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine
Generic Name venlafaxine
Labeler ascend laboratories, llc
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 37.5 mg/1

Manufacturer
Ascend Laboratories, LLC

Identifiers & Regulatory

Product NDC 67877-726
Product ID 67877-726_17943f8a-6ea6-4e86-93cc-df580774a8d9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214127
Listing Expiration 2026-12-31
Marketing Start 2021-06-11

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 67877726
Hyphenated Format 67877-726

Supplemental Identifiers

RxCUI
808744 808748 808751 808753
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 (source: ndc)
Generic Name venlafaxine (source: ndc)
Application Number ANDA214127 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 37.5 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-726-30)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-726-90)
source: ndc

Packages (2)

67877-726-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-726-30) 67877-726-90 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-726-90)

Ingredients (1)

venlafaxine hydrochloride (37.5 mg/1)

Linked Drug Pages (1)

Venlafaxine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "17943f8a-6ea6-4e86-93cc-df580774a8d9", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["808744", "808748", "808751", "808753"], "spl_set_id": ["528d5392-4ad5-48c5-963d-6ebfb9187db4"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-726-30)", "package_ndc": "67877-726-30", "marketing_start_date": "20210611"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-726-90)", "package_ndc": "67877-726-90", "marketing_start_date": "20210611"}], "brand_name": "Venlafaxine", "product_id": "67877-726_17943f8a-6ea6-4e86-93cc-df580774a8d9", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "67877-726", "generic_name": "Venlafaxine", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA214127", "marketing_category": "ANDA", "marketing_start_date": "20210611", "listing_expiration_date": "20261231"}