Package 68071-1906-9

Brand: citalopram hydrobromide

Generic: citalopram hydrobromide
NDC Package

Package Facts

Identity

Package NDC 68071-1906-9
Digits Only 6807119069
Product NDC 68071-1906
Product ID 68071-1906_1cffeedf-9727-4dbe-e063-6394a90a2326
Description

90 TABLET in 1 BOTTLE (68071-1906-9)

Marketing

Marketing Status
Marketed Since 2017-08-25
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": "1cffeedf-9727-4dbe-e063-6394a90a2326", "openfda": {"upc": ["0368071190694"], "unii": ["I1E9D14F36"], "rxcui": ["200371"], "spl_set_id": ["579836d8-64ed-de2d-e053-2a91aa0a8392"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-1906-3)", "package_ndc": "68071-1906-3", "marketing_start_date": "20170825"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68071-1906-6)", "package_ndc": "68071-1906-6", "marketing_start_date": "20170825"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-1906-9)", "package_ndc": "68071-1906-9", "marketing_start_date": "20170825"}], "brand_name": "Citalopram Hydrobromide", "product_id": "68071-1906_1cffeedf-9727-4dbe-e063-6394a90a2326", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68071-1906", "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": "20 mg/1"}], "application_number": "ANDA078216", "marketing_category": "ANDA", "marketing_start_date": "20071018", "listing_expiration_date": "20261231"}