venlafaxine

Generic: venlafaxine

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine
Generic Name venlafaxine
Labeler american health packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 75 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 68084-856
Product ID 68084-856_1f401c77-b3c1-291d-e063-6394a90aa890
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077653
Listing Expiration 2026-12-31
Marketing Start 2015-03-06

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 68084856
Hyphenated Format 68084-856

Supplemental Identifiers

RxCUI
313582 313584 313586
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 (source: ndc)
Generic Name venlafaxine (source: ndc)
Application Number ANDA077653 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-856-01) / 1 TABLET in 1 BLISTER PACK (68084-856-11)
source: ndc

Packages (1)

68084-856-01 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-856-01) / 1 TABLET in 1 BLISTER PACK (68084-856-11)

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": "1f401c77-b3c1-291d-e063-6394a90aa890", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313582", "313584", "313586"], "spl_set_id": ["d8899628-6e1b-40c6-9bc8-553d91ae2d0c"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-856-01)  / 1 TABLET in 1 BLISTER PACK (68084-856-11)", "package_ndc": "68084-856-01", "marketing_start_date": "20150306"}], "brand_name": "Venlafaxine", "product_id": "68084-856_1f401c77-b3c1-291d-e063-6394a90aa890", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68084-856", "generic_name": "Venlafaxine", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA077653", "marketing_category": "ANDA", "marketing_start_date": "20150306", "listing_expiration_date": "20261231"}