venlafaxine hydrochloride

Generic: venlafaxine hydrochloride

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

Drug Facts

Product Profile

Brand Name venlafaxine hydrochloride
Generic Name venlafaxine hydrochloride
Labeler american health packaging
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 37.5 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 68084-698
Product ID 68084-698_38559313-5695-06b2-e063-6394a90a92f2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200834
Listing Expiration 2026-12-31
Marketing Start 2014-02-06

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 68084698
Hyphenated Format 68084-698

Supplemental Identifiers

RxCUI
313581 313583 313585
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 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 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-698-01) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (68084-698-11)
source: ndc

Packages (1)

68084-698-01 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-698-01) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (68084-698-11)

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": "38559313-5695-06b2-e063-6394a90a92f2", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313581", "313583", "313585"], "spl_set_id": ["e05bdeb4-07a9-441e-901b-f2aea550db2b"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-698-01)  / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (68084-698-11)", "package_ndc": "68084-698-01", "marketing_start_date": "20140206"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "68084-698_38559313-5695-06b2-e063-6394a90a92f2", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68084-698", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "American Health Packaging", "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": "20140206", "listing_expiration_date": "20261231"}