venlafaxine hydrochloride

Generic: venlafaxine hydrochloride

Labeler: dr.reddys laboratories inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine hydrochloride
Generic Name venlafaxine hydrochloride
Labeler dr.reddys laboratories inc
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 75 mg/1

Manufacturer
Dr.Reddys Laboratories Inc

Identifiers & Regulatory

Product NDC 43598-001
Product ID 43598-001_646ca48a-403a-0ef0-0fc2-a5569c5b70fd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078421
Listing Expiration 2026-12-31
Marketing Start 2024-09-09

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 43598001
Hyphenated Format 43598-001

Supplemental Identifiers

RxCUI
313581 313583 313585
UPC
0343598001302 0343598999302
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 ANDA078421 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43598-001-10)
  • 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43598-001-30)
  • 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43598-001-90)
source: ndc

Packages (3)

43598-001-10 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43598-001-10) 43598-001-30 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43598-001-30) 43598-001-90 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43598-001-90)

Ingredients (1)

venlafaxine hydrochloride (75 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": "646ca48a-403a-0ef0-0fc2-a5569c5b70fd", "openfda": {"upc": ["0343598001302", "0343598999302"], "unii": ["7D7RX5A8MO"], "rxcui": ["313581", "313583", "313585"], "spl_set_id": ["f5c21429-d5d0-9f93-a465-6e5e0e19ebdd"], "manufacturer_name": ["Dr.Reddys Laboratories Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43598-001-10)", "package_ndc": "43598-001-10", "marketing_start_date": "20240909"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43598-001-30)", "package_ndc": "43598-001-30", "marketing_start_date": "20240909"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43598-001-90)", "package_ndc": "43598-001-90", "marketing_start_date": "20240909"}], "brand_name": "venlafaxine hydrochloride", "product_id": "43598-001_646ca48a-403a-0ef0-0fc2-a5569c5b70fd", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "43598-001", "generic_name": "venlafaxine hydrochloride", "labeler_name": "Dr.Reddys Laboratories Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA078421", "marketing_category": "ANDA", "marketing_start_date": "20240909", "listing_expiration_date": "20261231"}