Package 60760-836-30

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-836-30
Digits Only 6076083630
Product NDC 60760-836
Product ID 60760-836_35d31421-2856-1e64-e063-6294a90a9ccd
Description

30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-836-30)

Marketing

Marketing Status
Marketed Since 2025-05-13
Brand venlafaxine hydrochloride
Generic venlafaxine hydrochloride
Sample Package No

Linked Drug Pages (1)

Venlafaxine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "35d31421-2856-1e64-e063-6294a90a9ccd", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313583"], "spl_set_id": ["35d3148b-52f3-197c-e063-6294a90a44e3"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-836-30)", "package_ndc": "60760-836-30", "marketing_start_date": "20250513"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "60760-836_35d31421-2856-1e64-e063-6294a90a9ccd", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "60760-836", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "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": "20110601", "listing_expiration_date": "20261231"}