citalopram

Generic: citalopram hydrobromide

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name citalopram
Generic Name citalopram hydrobromide
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

citalopram hydrobromide 20 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-679
Product ID 63187-679_4b2a9a90-3ac3-4386-8772-64b4b9a86b28
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077031
Listing Expiration 2026-12-31
Marketing Start 2004-10-28

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63187679
Hyphenated Format 63187-679

Supplemental Identifiers

RxCUI
200371
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 hydrobromide (source: ndc)
Application Number ANDA077031 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (63187-679-00)
  • 30 TABLET, FILM COATED in 1 BOTTLE (63187-679-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (63187-679-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (63187-679-90)
source: ndc

Packages (4)

63187-679-00 100 TABLET, FILM COATED in 1 BOTTLE (63187-679-00) 63187-679-30 30 TABLET, FILM COATED in 1 BOTTLE (63187-679-30) 63187-679-60 60 TABLET, FILM COATED in 1 BOTTLE (63187-679-60) 63187-679-90 90 TABLET, FILM COATED in 1 BOTTLE (63187-679-90)

Ingredients (1)

citalopram hydrobromide (20 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": "4b2a9a90-3ac3-4386-8772-64b4b9a86b28", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["200371"], "spl_set_id": ["289c1d5e-902f-47db-85b8-5e1a55ec8684"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (63187-679-00)", "package_ndc": "63187-679-00", "marketing_start_date": "20160401"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63187-679-30)", "package_ndc": "63187-679-30", "marketing_start_date": "20160401"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (63187-679-60)", "package_ndc": "63187-679-60", "marketing_start_date": "20160401"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (63187-679-90)", "package_ndc": "63187-679-90", "marketing_start_date": "20160401"}], "brand_name": "Citalopram", "product_id": "63187-679_4b2a9a90-3ac3-4386-8772-64b4b9a86b28", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "63187-679", "generic_name": "Citalopram Hydrobromide", "labeler_name": "Proficient Rx LP", "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"}