Package 60760-009-30

Brand: citalopram hydrobromide

Generic: citalopram hydrobromide
NDC Package

Package Facts

Identity

Package NDC 60760-009-30
Digits Only 6076000930
Product NDC 60760-009
Description

30 TABLET in 1 BOTTLE, PLASTIC (60760-009-30)

Marketing

Marketing Status
Marketed Since 2007-10-18
Brand citalopram hydrobromide
Generic citalopram hydrobromide
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ded44f64-c51c-1454-e053-2995a90a908c", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["283672"], "spl_set_id": ["351ca54b-0eb6-4e93-8ab4-82fb18dcc9e1"], "manufacturer_name": ["St Marys Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (60760-009-30)", "package_ndc": "60760-009-30", "marketing_start_date": "20071018"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (60760-009-90)", "package_ndc": "60760-009-90", "marketing_start_date": "20071018"}], "brand_name": "Citalopram Hydrobromide", "product_id": "60760-009_ded44f64-c51c-1454-e053-2995a90a908c", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "60760-009", "generic_name": "Citalopram Hydrobromide", "labeler_name": "St Marys Medical Park Pharmacy", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram Hydrobromide", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "10 mg/1"}], "application_number": "ANDA078216", "marketing_category": "ANDA", "marketing_start_date": "20071018", "listing_expiration_date": "20261231"}