citalopram

Generic: citalopram

Labeler: aphena pharma solutions - tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name citalopram
Generic Name citalopram
Labeler aphena pharma solutions - tennessee, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

citalopram hydrobromide 40 mg/1

Manufacturer
Aphena Pharma Solutions - Tennessee, LLC

Identifiers & Regulatory

Product NDC 71610-422
Product ID 71610-422_5b7791df-471c-4407-a795-ad43aba3142d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077045
Listing Expiration 2026-12-31
Marketing Start 2011-05-20

Pharmacologic Class

Classes
serotonin reuptake inhibitor [epc] serotonin uptake inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71610422
Hyphenated Format 71610-422

Supplemental Identifiers

RxCUI
309314
UNII
I1E9D14F36

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name citalopram (source: ndc)
Generic Name citalopram (source: ndc)
Application Number ANDA077045 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 45 TABLET, FILM COATED in 1 BOTTLE (71610-422-45)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71610-422-60)
source: ndc

Packages (2)

71610-422-45 45 TABLET, FILM COATED in 1 BOTTLE (71610-422-45) 71610-422-60 90 TABLET, FILM COATED in 1 BOTTLE (71610-422-60)

Ingredients (1)

citalopram hydrobromide (40 mg/1)

Linked Drug Pages (1)

Citalopram ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5b7791df-471c-4407-a795-ad43aba3142d", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["309314"], "spl_set_id": ["3d70380f-ef97-4de9-a8f8-44ef9ba7e5a7"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "45 TABLET, FILM COATED in 1 BOTTLE (71610-422-45)", "package_ndc": "71610-422-45", "marketing_start_date": "20200501"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71610-422-60)", "package_ndc": "71610-422-60", "marketing_start_date": "20200518"}], "brand_name": "Citalopram", "product_id": "71610-422_5b7791df-471c-4407-a795-ad43aba3142d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71610-422", "generic_name": "Citalopram", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "40 mg/1"}], "application_number": "ANDA077045", "marketing_category": "ANDA", "marketing_start_date": "20110520", "listing_expiration_date": "20261231"}