venlafaxine

Generic: venlafaxine hydrochloride

Labeler: rising pharma holdings, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine
Generic Name venlafaxine hydrochloride
Labeler rising pharma holdings, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 75 mg/1

Manufacturer
Rising Pharma Holdings, Inc.

Identifiers & Regulatory

Product NDC 57237-175
Product ID 57237-175_4da7fe70-bb28-43f2-97b6-66d130e6c72f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090555
Listing Expiration 2026-12-31
Marketing Start 2010-04-07

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 57237175
Hyphenated Format 57237-175

Supplemental Identifiers

RxCUI
313580 313582 313584 313586 314277
UPC
0357237176900 0357237172902 0357237174906 0357237175903 0357237173909
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 hydrochloride (source: ndc)
Application Number ANDA090555 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (57237-175-01)
  • 90 TABLET in 1 BOTTLE (57237-175-90)
source: ndc

Packages (2)

57237-175-01 100 TABLET in 1 BOTTLE (57237-175-01) 57237-175-90 90 TABLET in 1 BOTTLE (57237-175-90)

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": "4da7fe70-bb28-43f2-97b6-66d130e6c72f", "openfda": {"upc": ["0357237176900", "0357237172902", "0357237174906", "0357237175903", "0357237173909"], "unii": ["7D7RX5A8MO"], "rxcui": ["313580", "313582", "313584", "313586", "314277"], "spl_set_id": ["20319949-ccf9-477a-a6e3-53502772deb9"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (57237-175-01)", "package_ndc": "57237-175-01", "marketing_start_date": "20100407"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (57237-175-90)", "package_ndc": "57237-175-90", "marketing_start_date": "20100407"}], "brand_name": "venlafaxine", "product_id": "57237-175_4da7fe70-bb28-43f2-97b6-66d130e6c72f", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "57237-175", "generic_name": "venlafaxine hydrochloride", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA090555", "marketing_category": "ANDA", "marketing_start_date": "20100407", "listing_expiration_date": "20261231"}