venlafaxine hydrochloride

Generic: venlafaxine hydrochloride

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine hydrochloride
Generic Name venlafaxine hydrochloride
Labeler aurobindo pharma limited
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 37.5 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 65862-527
Product ID 65862-527_d3f9b554-05be-484f-b9e7-5c8e6b2de9c9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200834
Listing Expiration 2026-12-31
Marketing Start 2011-06-01

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 65862527
Hyphenated Format 65862-527

Supplemental Identifiers

RxCUI
313581 313583 313585
UPC
0365862528476 0365862527479
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 hydrochloride (source: ndc)
Generic Name venlafaxine hydrochloride (source: ndc)
Application Number ANDA200834 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 37.5 mg/1
source: ndc
Packaging
  • 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-527-01)
  • 10 BLISTER PACK in 1 CARTON (65862-527-10) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK
  • 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-527-30)
  • 15 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-527-47)
  • 5000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-527-59)
  • 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-527-90)
  • 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-527-99)
source: ndc

Packages (7)

65862-527-01 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-527-01) 65862-527-10 10 BLISTER PACK in 1 CARTON (65862-527-10) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK 65862-527-30 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-527-30) 65862-527-47 15 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-527-47) 65862-527-59 5000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-527-59) 65862-527-90 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-527-90) 65862-527-99 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-527-99)

Ingredients (1)

venlafaxine hydrochloride (37.5 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": "d3f9b554-05be-484f-b9e7-5c8e6b2de9c9", "openfda": {"upc": ["0365862528476", "0365862527479"], "unii": ["7D7RX5A8MO"], "rxcui": ["313581", "313583", "313585"], "spl_set_id": ["85d3ce8b-8966-45d9-bdaf-f6f0475096e1"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-527-01)", "package_ndc": "65862-527-01", "marketing_start_date": "20110601"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (65862-527-10)  / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "65862-527-10", "marketing_start_date": "20110601"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-527-30)", "package_ndc": "65862-527-30", "marketing_start_date": "20110601"}, {"sample": false, "description": "15 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-527-47)", "package_ndc": "65862-527-47", "marketing_start_date": "20110601"}, {"sample": false, "description": "5000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-527-59)", "package_ndc": "65862-527-59", "marketing_start_date": "20110601"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-527-90)", "package_ndc": "65862-527-90", "marketing_start_date": "20110601"}, {"sample": false, "description": "1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-527-99)", "package_ndc": "65862-527-99", "marketing_start_date": "20110601"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "65862-527_d3f9b554-05be-484f-b9e7-5c8e6b2de9c9", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "65862-527", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA200834", "marketing_category": "ANDA", "marketing_start_date": "20110601", "listing_expiration_date": "20261231"}