Package 43063-661-90

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 43063-661-90
Digits Only 4306366190
Product NDC 43063-661
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-661-90)

Marketing

Marketing Status
Marketed Since 2016-03-03
Brand escitalopram
Generic escitalopram
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b375aaf-89c3-643b-e063-6294a90a6ee0", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351250"], "spl_set_id": ["2d125ea4-5430-5b4e-e054-00144ff88e88"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-661-30)", "package_ndc": "43063-661-30", "marketing_start_date": "20160303"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-661-90)", "package_ndc": "43063-661-90", "marketing_start_date": "20160303"}], "brand_name": "Escitalopram", "product_id": "43063-661_2b375aaf-89c3-643b-e063-6294a90a6ee0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "43063-661", "generic_name": "Escitalopram", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "20 mg/1"}], "application_number": "ANDA202389", "marketing_category": "ANDA", "marketing_start_date": "20130321", "listing_expiration_date": "20261231"}