Package 42708-194-30

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package Sample

Package Facts

Identity

Package NDC 42708-194-30
Digits Only 4270819430
Product NDC 42708-194
Product ID 42708-194_499278ff-59b6-7393-e063-6394a90adf5d
Description

30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (42708-194-30)

Marketing

Marketing Status
Marketed Since 2026-02-01
Brand venlafaxine hydrochloride
Generic venlafaxine hydrochloride
Sample Package Yes

Linked Drug Pages (1)

Venlafaxine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "499278ff-59b6-7393-e063-6394a90adf5d", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313585"], "spl_set_id": ["4992698e-5d5a-6468-e063-6394a90ab404"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (42708-194-30)", "package_ndc": "42708-194-30", "marketing_start_date": "20260201"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "42708-194_499278ff-59b6-7393-e063-6394a90adf5d", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "42708-194", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "QPharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA200834", "marketing_category": "ANDA", "marketing_start_date": "20110601", "listing_expiration_date": "20271231"}