Package 68071-3384-1

Brand: citalopram hydrobromide

Generic: citalopram hydrobromide
NDC Package

Package Facts

Identity

Package NDC 68071-3384-1
Digits Only 6807133841
Product NDC 68071-3384
Product ID 68071-3384_1ce93198-902a-e4f5-e063-6294a90a3294
Description

100 TABLET in 1 BOTTLE (68071-3384-1)

Marketing

Marketing Status
Marketed Since 2017-07-18
Brand citalopram hydrobromide
Generic citalopram hydrobromide
Sample Package No

Linked Drug Pages (1)

Citalopram Hydrobromide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1ce93198-902a-e4f5-e063-6294a90a3294", "openfda": {"upc": ["0368071338416"], "unii": ["I1E9D14F36"], "rxcui": ["309314"], "spl_set_id": ["549a5b3f-4928-1ae5-e054-00144ff8d46c"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68071-3384-1)", "package_ndc": "68071-3384-1", "marketing_start_date": "20170718"}], "brand_name": "Citalopram Hydrobromide", "product_id": "68071-3384_1ce93198-902a-e4f5-e063-6294a90a3294", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68071-3384", "generic_name": "Citalopram Hydrobromide", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram Hydrobromide", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "40 mg/1"}], "application_number": "ANDA078216", "marketing_category": "ANDA", "marketing_start_date": "20071018", "listing_expiration_date": "20261231"}