Package 70518-2228-0

Brand: citalopram

Generic: citalopram
NDC Package

Package Facts

Identity

Package NDC 70518-2228-0
Digits Only 7051822280
Product NDC 70518-2228
Description

30 TABLET in 1 BLISTER PACK (70518-2228-0)

Marketing

Marketing Status
Marketed Since 2019-07-13
Brand citalopram
Generic citalopram
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4ba688dd-17ac-975f-e063-6394a90aef14", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["309314"], "spl_set_id": ["c9809dfe-939e-4f9d-b6dd-f9808fd9f2b1"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2228-0)", "package_ndc": "70518-2228-0", "marketing_start_date": "20190713"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-2228-1)", "package_ndc": "70518-2228-1", "marketing_start_date": "20191005"}], "brand_name": "Citalopram", "product_id": "70518-2228_4ba688dd-17ac-975f-e063-6394a90aef14", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-2228", "generic_name": "Citalopram", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "40 mg/1"}], "application_number": "ANDA077534", "marketing_category": "ANDA", "marketing_start_date": "20190713", "listing_expiration_date": "20271231"}