Package 42708-019-30

Brand: citalopram

Generic: citalopram hydrobromide
NDC Package Sample

Package Facts

Identity

Package NDC 42708-019-30
Digits Only 4270801930
Product NDC 42708-019
Product ID 42708-019_45866b17-f905-ad71-e063-6394a90a9455
Description

30 TABLET, FILM COATED in 1 BOTTLE (42708-019-30)

Marketing

Marketing Status
Marketed Since 2018-03-14
Brand citalopram
Generic citalopram hydrobromide
Sample Package Yes

Linked Drug Pages (1)

Citalopram ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "45866b17-f905-ad71-e063-6394a90a9455", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["200371"], "spl_set_id": ["0a967468-3869-4c8c-849f-9fc3a8dcc489"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET, FILM COATED in 1 BOTTLE (42708-019-30)", "package_ndc": "42708-019-30", "marketing_start_date": "20180314"}], "brand_name": "Citalopram", "product_id": "42708-019_45866b17-f905-ad71-e063-6394a90a9455", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "42708-019", "generic_name": "Citalopram Hydrobromide", "labeler_name": "QPharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "20 mg/1"}], "application_number": "ANDA077031", "marketing_category": "ANDA", "marketing_start_date": "20041028", "listing_expiration_date": "20261231"}