venlafaxine

Generic: venlafaxine

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

Drug Facts

Product Profile

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

venlafaxine hydrochloride 75 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0778
Product ID 71335-0778_a90443c0-5875-46af-857d-1fdae8c8ad0e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078932
Listing Expiration 2026-12-31
Marketing Start 2015-10-01

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 713350778
Hyphenated Format 71335-0778

Supplemental Identifiers

RxCUI
313586
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 (source: ndc)
Generic Name venlafaxine (source: ndc)
Application Number ANDA078932 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (71335-0778-1)
  • 30 TABLET in 1 BOTTLE (71335-0778-2)
  • 90 TABLET in 1 BOTTLE (71335-0778-3)
  • 28 TABLET in 1 BOTTLE (71335-0778-4)
  • 120 TABLET in 1 BOTTLE (71335-0778-5)
  • 100 TABLET in 1 BOTTLE (71335-0778-6)
source: ndc

Packages (6)

71335-0778-1 60 TABLET in 1 BOTTLE (71335-0778-1) 71335-0778-2 30 TABLET in 1 BOTTLE (71335-0778-2) 71335-0778-3 90 TABLET in 1 BOTTLE (71335-0778-3) 71335-0778-4 28 TABLET in 1 BOTTLE (71335-0778-4) 71335-0778-5 120 TABLET in 1 BOTTLE (71335-0778-5) 71335-0778-6 100 TABLET in 1 BOTTLE (71335-0778-6)

Ingredients (1)

venlafaxine hydrochloride (75 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": "a90443c0-5875-46af-857d-1fdae8c8ad0e", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313586"], "spl_set_id": ["0c9511a2-c581-44cd-bf38-a751fcc658e4"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-0778-1)", "package_ndc": "71335-0778-1", "marketing_start_date": "20220209"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0778-2)", "package_ndc": "71335-0778-2", "marketing_start_date": "20220209"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0778-3)", "package_ndc": "71335-0778-3", "marketing_start_date": "20220209"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-0778-4)", "package_ndc": "71335-0778-4", "marketing_start_date": "20220209"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-0778-5)", "package_ndc": "71335-0778-5", "marketing_start_date": "20220209"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-0778-6)", "package_ndc": "71335-0778-6", "marketing_start_date": "20220209"}], "brand_name": "venlafaxine", "product_id": "71335-0778_a90443c0-5875-46af-857d-1fdae8c8ad0e", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "71335-0778", "generic_name": "venlafaxine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA078932", "marketing_category": "ANDA", "marketing_start_date": "20151001", "listing_expiration_date": "20261231"}