Package 0093-1024-06

Brand: nefazodone hydrochloride

Generic: nefazodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0093-1024-06
Digits Only 0093102406
Product NDC 0093-1024
Product ID 0093-1024_11cdc932-271c-4988-aad9-076340888bce
Description

60 TABLET in 1 BOTTLE (0093-1024-06)

Marketing

Marketing Status
Marketed Since 2003-09-16
Brand nefazodone hydrochloride
Generic nefazodone hydrochloride
Sample Package No

Linked Drug Pages (1)

Nefazodone Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "11cdc932-271c-4988-aad9-076340888bce", "openfda": {"upc": ["0300931024060", "0300937113065"], "unii": ["27X63J94GR"], "rxcui": ["1098649", "1098666", "1098670", "1098674", "1098678"], "spl_set_id": ["51ff7db5-aaf9-4c3c-86e6-958ebf16b60f"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (0093-1024-06)", "package_ndc": "0093-1024-06", "marketing_start_date": "20030916"}], "brand_name": "Nefazodone Hydrochloride", "product_id": "0093-1024_11cdc932-271c-4988-aad9-076340888bce", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "0093-1024", "generic_name": "Nefazodone Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nefazodone Hydrochloride", "active_ingredients": [{"name": "NEFAZODONE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA076037", "marketing_category": "ANDA", "marketing_start_date": "20030916", "listing_expiration_date": "20261231"}