venlafaxine hcl er

Generic: venlafaxine hcl er

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine hcl er
Generic Name venlafaxine hcl er
Labeler direct_rx
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 37.5 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-363
Product ID 72189-363_2c4c85cc-c2bb-ac98-e063-6294a90a973c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200834
Listing Expiration 2026-12-31
Marketing Start 2022-06-22

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 72189363
Hyphenated Format 72189-363

Supplemental Identifiers

RxCUI
313583
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 hcl er (source: ndc)
Generic Name venlafaxine hcl er (source: ndc)
Application Number ANDA200834 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 37.5 mg/1
source: ndc
Packaging
  • 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72189-363-30)
  • 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72189-363-60)
source: ndc

Packages (2)

72189-363-30 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72189-363-30) 72189-363-60 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72189-363-60)

Ingredients (1)

venlafaxine hydrochloride (37.5 mg/1)

Linked Drug Pages (1)

Venlafaxine HCL ER ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c4c85cc-c2bb-ac98-e063-6294a90a973c", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313583"], "spl_set_id": ["e20b7d9e-f755-4325-e053-2995a90ac45d"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72189-363-30)", "package_ndc": "72189-363-30", "marketing_start_date": "20220826"}, {"sample": false, "description": "60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72189-363-60)", "package_ndc": "72189-363-60", "marketing_start_date": "20220622"}], "brand_name": "Venlafaxine HCL ER", "product_id": "72189-363_2c4c85cc-c2bb-ac98-e063-6294a90a973c", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "72189-363", "generic_name": "Venlafaxine HCL ER", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine HCL ER", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA200834", "marketing_category": "ANDA", "marketing_start_date": "20220622", "listing_expiration_date": "20261231"}