venlafaxine hydrochloride

Generic: venlafaxine hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine hydrochloride
Generic Name venlafaxine hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 150 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 63629-2100
Product ID 63629-2100_c03a4815-4a12-4abb-aa11-0b1b078929da
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209193
Listing Expiration 2026-12-31
Marketing Start 2019-10-31

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 636292100
Hyphenated Format 63629-2100

Supplemental Identifiers

RxCUI
808744
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 ANDA209193 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (63629-2100-1)
source: ndc

Packages (1)

63629-2100-1 30 TABLET in 1 BOTTLE (63629-2100-1)

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": "c03a4815-4a12-4abb-aa11-0b1b078929da", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["808744"], "spl_set_id": ["5d184d1b-67fe-4965-bf3d-b49646df4f92"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (63629-2100-1)", "package_ndc": "63629-2100-1", "marketing_start_date": "20191031"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "63629-2100_c03a4815-4a12-4abb-aa11-0b1b078929da", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "63629-2100", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA209193", "marketing_category": "ANDA", "marketing_start_date": "20191031", "listing_expiration_date": "20261231"}