Package 0904-6426-61

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 0904-6426-61
Digits Only 0904642661
Product NDC 0904-6426
Product ID 0904-6426_6dd4eb62-4211-41c7-8592-69c0b045b53f
Description

100 BLISTER PACK in 1 CARTON (0904-6426-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2014-10-15
Brand escitalopram
Generic escitalopram
Sample Package No

Linked Drug Pages (1)

escitalopram ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6dd4eb62-4211-41c7-8592-69c0b045b53f", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["349332", "351250"], "spl_set_id": ["f4a12048-181e-45ed-a382-f53096d1b689"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6426-61)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6426-61", "marketing_start_date": "20141015"}], "brand_name": "escitalopram", "product_id": "0904-6426_6dd4eb62-4211-41c7-8592-69c0b045b53f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "0904-6426", "generic_name": "escitalopram", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "10 mg/1"}], "application_number": "ANDA090939", "marketing_category": "ANDA", "marketing_start_date": "20141015", "listing_expiration_date": "20271231"}