Package 60760-304-30

Brand: venlafaxine

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-304-30
Digits Only 6076030430
Product NDC 60760-304
Product ID 60760-304_a97d917a-6b6e-b9bd-e053-2a95a90afcce
Description

30 TABLET in 1 BOTTLE, PLASTIC (60760-304-30)

Marketing

Marketing Status
Marketed Since 2020-06-16
Brand venlafaxine
Generic venlafaxine hydrochloride
Sample Package No

Linked Drug Pages (1)

venlafaxine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a97d917a-6b6e-b9bd-e053-2a95a90afcce", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313586"], "spl_set_id": ["a97dbc5e-7c19-58f9-e053-2995a90a1ad0"], "manufacturer_name": ["St. Mary's Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (60760-304-30)", "package_ndc": "60760-304-30", "marketing_start_date": "20200616"}], "brand_name": "venlafaxine", "product_id": "60760-304_a97d917a-6b6e-b9bd-e053-2a95a90afcce", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "60760-304", "generic_name": "venlafaxine hydrochloride", "labeler_name": "St. Mary's Medical Park Pharmacy", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA090555", "marketing_category": "ANDA", "marketing_start_date": "20200616", "listing_expiration_date": "20261231"}