venlafaxine
Generic: venlafaxine
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
venlafaxine
Generic Name
venlafaxine
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
venlafaxine hydrochloride 37.5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-9704
Product ID
71335-9704_1471508e-7fe4-43db-94ea-b4df1bcbafa9
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077653
Listing Expiration
2026-12-31
Marketing Start
2008-06-13
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713359704
Hyphenated Format
71335-9704
Supplemental Identifiers
RxCUI
UNII
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
ANDA077653 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 37.5 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (71335-9704-1)
- 60 TABLET in 1 BOTTLE (71335-9704-2)
- 90 TABLET in 1 BOTTLE (71335-9704-3)
- 10 TABLET in 1 BOTTLE (71335-9704-4)
Packages (4)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1471508e-7fe4-43db-94ea-b4df1bcbafa9", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313584"], "spl_set_id": ["1471508e-7fe4-43db-94ea-b4df1bcbafa9"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-9704-1)", "package_ndc": "71335-9704-1", "marketing_start_date": "20230424"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-9704-2)", "package_ndc": "71335-9704-2", "marketing_start_date": "20230627"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-9704-3)", "package_ndc": "71335-9704-3", "marketing_start_date": "20231010"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (71335-9704-4)", "package_ndc": "71335-9704-4", "marketing_start_date": "20240405"}], "brand_name": "Venlafaxine", "product_id": "71335-9704_1471508e-7fe4-43db-94ea-b4df1bcbafa9", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "71335-9704", "generic_name": "Venlafaxine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA077653", "marketing_category": "ANDA", "marketing_start_date": "20080613", "listing_expiration_date": "20261231"}